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Index of chemical compounds with the same name
Diphenol may refer to: Benzenediols Bisphenols Dihydroxybiphenyls Various polyphenols (those with 2 phenolic groups) This set index article lists chemical
Diphenol
Chemical used in plastics, xenoestrogen
et al. (May 2004). "Impurities in industrial grade 4,4'-isopropylidene diphenol (bisphenol A): possible implications for estrogenic activity". Chemosphere
Bisphenol_A
Organic compound (C6H5OH)
polycarbonates and epoxide resins. Condensation of phenol, alkylphenols, or diphenols with formaldehyde gives phenolic resins, an example of which is Bakelite
Phenol
Chemical compound
Salen ligand Names Other names 2,2′-Ethylenebis(nitrilomethylidene)diphenol, N,N′-Ethylenebis(salicylimine) Identifiers CAS Number 129409-01-4 Y 94-93-9
Salen_ligand
Class of polymers
Function 4,4'-Dichlorodiphenyl sulfone 80-07-9 C₁₂H₈Cl₂O₂S Sulfone-containing dihalide monomer 4,4'-Biphenol 92-88-6 C₁₂H₁₀O₂ Aromatic diphenol monomer
Polyphenylenesulfone
Organic compound (C6H4(OH)2); benzene with two adjacent –OH groups
Catechol (/ˈkætɪtʃɒl/ or /ˈkætɪkɒl/), also known as pyrocatechol or 1,2-dihydroxybenzene, is an organic compound with the molecular formula C6H4(OH)2.
Catechol
Enzyme for controlling the production of melanin
the hydroxylation of a monophenol and secondly, the conversion of an o-diphenol to the corresponding o-quinone. o-Quinone undergoes several reactions to
Tyrosinase
Enzyme
contains a type 3 di-copper cofactor and catalyzes the oxidation of ortho-diphenols into ortho-quinones coupled with the reduction of molecular oxygen to
Catechol_oxidase
Index of chemical compounds with the same name
In organic chemistry, dihydroxybenzenes (benzenediols) are organic compounds in which two hydroxyl groups (−OH) are substituted onto a benzene ring (C6H6)
Dihydroxybenzenes
Enzyme involved in fruit browning
four atoms of copper per molecule. PPO may accept monophenols and/or o-diphenols as substrates. The enzyme works by catalyzing the o-hydroxylation of monophenol
Polyphenol_oxidase
Chemical compound
+ HOC6H5 → (HOC6H4)2CH2 + H2O 2 HOC6H4CH2OH → (HOC6H4CH2)2O + H2O The diphenol (HOC6H4)2CH2 (sometimes called a "dimer") is called bisphenol F, which
Phenol_formaldehyde_resin
Group of chemical compounds
Chemical structure of aloe emodin, a diphenol
Naturally_occurring_phenols
Chemical compound
hydragogue and laxative effect of the sulfuric acid ester and the free diphenol of 4,4'-dihydroxydiphenyl-(pyridyl-2)-methane". Naunyn-Schmiedeberg's Archives
Sodium_picosulfate
Class of high performance thermoplastic polymers
toward substitution. The required diphenoxide is produced in situ from a diphenol and sodium hydroxide. The cogenerated water is removed by azeotropic distillation
Polysulfone
Chemical compound
caffeic acid into ferulic acid. Caffeic acid and related o-diphenols are rapidly oxidized by o-diphenol oxidases in tissue extracts. Caffeate 3,4-dioxygenase
Caffeic_acid
Chemical compound
Names Preferred IUPAC name 4,4′-(1,1,1,3,3,3-Hexafluoropropane-2,2-diyl)diphenol Other names Biphenol AF; Hexafluorobisphenol A; Hexafluorodiphenylolpropane;
Bisphenol_AF
Chemical compound
name [1,1′-Biphenyl]-4,4′-diol Other names 4,4′-Dihydroxybiphenyl 4,4′-Diphenol 4,4′-Biphenyldiol Identifiers CAS Number 92-88-6 Y 3D model (JSmol) Interactive
4,4'-Biphenol
Species of bacterium
wastes on Sitia on Crete. Olivibacter sitiensis has the ability to degrade diphenol. Parte, A.C. "Olivibacter". LPSN. "Olivibacter sitiensis Taxon Passport
Olivibacter_sitiensis
Chemical compound
monoalkylated derivatives undergo coupling to give an extensive family of diphenol antioxidants. These antioxidants are valued because they are relatively
P-Cresol
Chemical compound
Names Preferred IUPAC name 4,4′-[(4-Hydroxy-1,3-phenylene)bis(methylene)]diphenol Identifiers CAS Number 34826-64-7 3D model (JSmol) Interactive image ChEMBL
2,4-Bis(4-hydroxybenzyl)phenol
2,4-Bis(4-hydroxybenzyl)phenol
Enzyme involved in redox reactions
on a heme group of donors EC 1.10 includes oxidoreductases that act on diphenols and related substances as donors EC 1.11 includes oxidoreductases that
Oxidoreductase
Chemical compound
Preferred IUPAC name 4,4′-[(1Z,3Z)-2,3-Diisocyanobuta-1,3-diene-1,4-diyl]diphenol Other names Xanthocillin X, Ophthocillin Identifiers CAS Number 580-74-5 Y
Xantocillin
Class of enzymes
belongs to the family of oxidoreductases, specifically those acting on diphenols and related substances as donor with a cytochrome as acceptor. This enzyme
Coenzyme Q – cytochrome c reductase
Coenzyme_Q_–_cytochrome_c_reductase
Chemical reaction
organic reaction of phenols with alkaline potassium persulfate to form para-diphenols. The reaction is generally performed in water at room temperatures or
Elbs_persulfate_oxidation
Enzyme
belongs to the family of oxidoreductases, specifically those acting on diphenols and related substances as donor with oxygen as acceptor. The systematic
Rifamycin-B_oxidase
Chemical compound
(SDA), while reaction with aminophenols yields the spirodilactam-diphenol (SDD). The diphenol derivative (SDD) in particular was used as a precursor for thermoplastics
1,6-Dioxaspiro(4.4)nonane-2,7-dione
1,6-Dioxaspiro(4.4)nonane-2,7-dione
Chemical compound
beginning with hydroxylation mediated by coniferyl aldehyde 5-hydroxylase. The diphenol is then methylated at the 5-OH by the action of caffeate O-methyltransferase
Sinapaldehyde
Norwegian chemical company
and lignin-based vanillin. The company also produces ethyl vanillin, diphenols and fine chemicals.[clarification needed] The name "Borregaard" was connected
Borregaard
Class of chemical compounds
Polyphenol oxidase (PPO) is an enzyme that catalyses the oxidation of o-diphenols to produce o-quinones. It is the rapid polymerisation of o-quinones to
Polyphenol
Indian chemicals manufacturer
Special Economic Zone in Gujarat and commenced commercial production at its diphenol manufacturing facility. The expansion increased the company's manufacturing
Camlin_Fine_Sciences
Class of enzymes
belongs to the family of oxidoreductases, specifically those acting on diphenols and related substances as donor with oxygen as acceptor. The systematic
3-hydroxyanthranilate_oxidase
Chemical compound
Names IUPAC name 2,2'-{1,2-Propanediylbis[nitrilo(E)methylylidene]}diphenol Identifiers CAS Number 94-91-7 Y 3D model (JSmol) Interactive image ChEMBL
Salpn_ligand
Enzymes are listed here by their classification in the International Union of Biochemistry and Molecular Biology's Enzyme Commission (EC) numbering system:
List_of_enzymes
Aromatic compounds containing Halogen atom(s) in place of Hydrogen
tetrabromobisphenol-A, which is prepared by direct bromination of the diphenol. Shimizu, Masaki; Hiyama, Tamejiro (2005). "Modern Synthetic Methods for
Aryl_halide
Chemical compound
Excretion Urine, feces Identifiers IUPAC name 4,4'-[(3E)-Hex-3-ene-3,4-diyl]diphenol CAS Number 56-53-1 Y PubChem CID 448537 IUPHAR/BPS 2801 DrugBank DB00255 Y
Diethylstilbestrol
Chemical compound
list (link) "RISK ASSESSMENT OF 2,2',6,6'-TETRABROMO-4,4'-ISOPROPYLIDENE DIPHENOL (TETRABROMOBISPHENOL-A)". Environment Agency (UK). June 2007. EFSA Scientific
Tetrabromobisphenol_A
Enzyme
belongs to the family of oxidoreductases, specifically those acting on diphenols and related substances as donor with NAD+ or NADP+ as acceptor. The systematic
Trans-acenaphthene-1,2-diol dehydrogenase
Trans-acenaphthene-1,2-diol_dehydrogenase
Protein-coding gene in humans
oxidoreductase activity aromatase activity oxidoreductase activity, acting on diphenols and related substances as donors monooxygenase activity estrogen 16-alpha-hydroxylase
CYP1A1
Chemical compound
Identifiers IUPAC name 4,4'-(1-(4-(2-Aminoethoxy)phenyl)but-1-ene-1,2-diyl)diphenol CAS Number 1946764-65-3 Y PubChem CID 159419575 ChemSpider 58967386 Chemical
4'-Hydroxynorendoxifen
Protein-coding gene in the species Homo sapiens
activity 2 iron, 2 sulfur cluster binding oxidoreductase activity, acting on diphenols and related substances as donors protein binding Cellular component integral
UQCRFS1
Chemical compound
complexes with di- and polyfunctional carboxylic acids, poly-alcohols, and o-diphenols. In contact with hydrochloric acid, it releases the volatile and corrosive
Germanium_dioxide
methyltransferase, luteolin methyltransferase, luteolin 3'-O-methyltransferase, o-diphenol m-O-methyltransferase, o-dihydric phenol meta-O-methyltransferase, and
Luteolin_O-methyltransferase
belongs to the family of oxidoreductases, specifically those acting on diphenols and related substances as donor with oxygen as acceptor. It participates
L-ascorbate_oxidase
Chemical compound
Dihydrodiethylstilbestrol; Dihydrostilbestrol; 4,4'-(1,2-Diethylethylene)diphenol; NSC-9894 Routes of administration By mouth, intramuscular injection (as
Hexestrol
Invertebrates defense system
PO catalyses a hydroxylation of monophenols (tyrosine) on diphenols and oxidation of diphenols to dichinones. The chinones non-enzymatically change their
Phenoloxidase_system
belongs to the family of oxidoreductases, specifically those acting on diphenols and related substances as donor with other acceptors. The systematic name
Ribosyldihydronicotinamide dehydrogenase (quinone)
Ribosyldihydronicotinamide_dehydrogenase_(quinone)
Russian chemist (1851–1918)
formation of triphenol I, 4,4'-(4-hydroxy-m-phenylenediisopropylidene)diphenol, from the attack of a carbenium electrophile on a bisphenol A molecule
Aleksandr_Dianin
Genus of bacteria
draft genome sequence of Olivibacter sitiensis type strain (AW-6T), a diphenol degrader with genes involved in the catechol pathway". Standards in Genomic
Olivibacter
Chemical compound
Stilbestrol Names Preferred IUPAC name 4,4′-[(E)-Ethene-1,2-diyl]diphenol Other names Dihydroxystilbene; 4,4'-Dihydroxystilbene, 4,4'-stilbenediol Identifiers
Stilbestrol
Chemical compound
HPTE Names Preferred IUPAC name 4,4′-(2,2,2-Trichloroethane-1,1-diyl)diphenol Other names p,p'-Hydroxy-DDT Hydroxychlor 2,2-bis(p-hydroxyphenyl)-1,1,1-trichloroethane
HPTE
This list contains a list of EC numbers for the first group, EC 1, oxidoreductases, placed in numerical order as determined by the Nomenclature Committee
List_of_EC_numbers_(EC_1)
Defunct chemical conglomerate
24% of Consumer Chemicals’ revenue. As the world's leading producer of diphenols, Aroma Performance supplies aromas and fragrances. Key products include
Rhodia_(company)
Romanian chemist
of energy resources. The first part, entitled "On the Constitution of Diphenol-, Dithiophenol-, Di-α- and β-Naphthol, Dithionaphthol, Dimethylaniline-
Constantin_Cândea
Swiss chemist (1899–1985)
he developed epoxy resins (From reaction between epichlorohydrin with diphenols), which he applied for in Switzerland in 1938 (granted 1940) (without
Pierre_Castan
Chemical compound
Names Preferred IUPAC name 4,4′-(4-Methylpent-1-ene-2,4-diyl)diphenol Identifiers CAS Number 13464-24-9 Y 3D model (JSmol) Interactive image
4-Methyl-2,4-bis(4-hydroxyphenyl)pent-1-ene
4-Methyl-2,4-bis(4-hydroxyphenyl)pent-1-ene
Chemical compound
through one electron. Metabolites formed in pathway III are mono- and diphenols. Similar to Pathway I, Pathway III proceeds via enzymatic catalysis, though
Anthanthrene
Chemical compound
Nonsteroidal estrogen Identifiers IUPAC name 4,4'-(3-ethylhexane-2,4-diyl)diphenol CAS Number 85-95-0 PubChem CID 6827 ChemSpider 6566 UNII A27512LR47 ChEBI
Benzestrol
Protein-coding gene in the species Homo sapiens
belongs to the family of oxidoreductases, specifically those acting on diphenols and related substances as donor with a cytochrome as acceptor. This enzyme
UQCR11
DIPHENOL
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Female
English
Feminine form of English unisex Ariel, ARIELLE means "lion of God."
Girl/Female
Bengali, Hindu, Indian, Kannada, Malayalam, Marathi, Sanskrit, Tamil, Telugu
Beautiful Picture
Girl/Female
Gaelic
Boy/Male
Australian, Indonesian
The Third Child
Boy/Male
Arabic
Commander; Head
Girl/Female
Muslim
Helper
Boy/Male
Muslim
The abaser
Female
Irish
Variant spelling of Irish Gaelic Muirgen, MUIRÃN means "born of the sea."
Girl/Female
American, Anglo, Australian, British, Chinese, English
Child of Mighty Warrior; Child of Maud; Matthew's Child
Female
Vietnamese
Vietnamese unisex name QUY means "precious."
DIPHENOL
DIPHENOL
DIPHENOL
DIPHENOL
DIPHENOL