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Details

Stereochemistry RACEMIC
Molecular Formula C8H10O2
Molecular Weight 138.1638
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of STYRENE GLYCOL

SMILES

OCC(O)C1=CC=CC=C1

InChI

InChIKey=PWMWNFMRSKOCEY-UHFFFAOYSA-N
InChI=1S/C8H10O2/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8-10H,6H2

HIDE SMILES / InChI

Molecular Formula C8H10O2
Molecular Weight 138.1638
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Trospium chloride--an effective drug in the treatment of overactive bladder and detrusor hyperreflexia.
2001 Nov
Liquid chromatography/electrospray tandem mass spectrometry characterization of styrene metabolism in man and in rat.
2002
Synthesis, biological, and chiroptical activity of 3-phenyl-clavams.
2004 Jan 15
Determination of absolute configuration of acyclic 1,2-diols with [Mo2(OAc)4], part 2: new structural evidence toward a rationale of the method: what remains of [Mo2(OAc)4] in DMSO solution?
2004 Mar 5
Preparation and evaluation of a chiral stationary phase covalently bound with chiral pseudo-1 8-crown-6 ether having 1-phenyl-1,2-cyclohexanediol as a chiral unit.
2005 Jun 17
Enzymatic resolution of racemic phenyloxirane by a novel epoxide hydrolase from Aspergillus niger SQ-6 and its fed-batch fermentation.
2006 Apr
Polymer supported vanadium and molybdenum complexes as potential catalysts for the oxidation and oxidative bromination of organic substrates.
2006 Aug 7
Synthesis, characterisation, reactivity and in vitro antiamoebic activity of hydrazone based oxovanadium(IV), oxovanadium(V) and mu-bis(oxo)bis{oxovanadium(V)} complexes.
2006 Feb 21
Enantioconvergent production of (R)-1-phenyl-1,2-ethanediol from styrene oxide by combining the Solanum tuberosum and an evolved Agrobacterium radiobacter AD1 epoxide hydrolases.
2006 Jun 20
New phenyl-ethanediols from the culture broth of Boletus edulis.
2007 Apr
A novel NADH-dependent carbonyl reductase with unusual stereoselectivity for (R)-specific reduction from an (S)-1-phenyl-1,2-ethanediol-producing micro-organism: purification and characterization.
2007 May
A catalytic one-step process for the chemo- and regioselective acylation of monosaccharides.
2007 Oct 24
Crystal structure of a carbonyl reductase from Candida parapsilosis with anti-Prelog stereospecificity.
2008 Aug
[Co-expression of formate dehydrogenase from Candida boidinii and (R)-specific carbonyl reductase from Candida parapsilosis CCTCC M203011 in Escherichia coli].
2008 Dec
Biosynthesis of (R)-phenyl-1,2-ethanediol from racemic styrene oxide by using bacterial and marine fish epoxide hydrolases.
2008 Jan
Screening enantioselective epoxide hydrolase activities from marine microorganisms: detection of activities in Erythrobacter spp.
2008 Jul-Aug
Cloning and characterization of an epoxide hydrolase from Novosphingobium aromaticivorans.
2009 Apr
[Improved expression and catalytic efficiency of (R)-carbonyl reductase in Escherichia coli by secondary structure optimization of mRNA translation initiation region].
2009 Dec
[Construction of an enzyme-coupled system consisting of (R)- and (S)-specific carbonyl reductases for one-step preparation of (S)-1-phenyl-1,2-ethanediol].
2009 Feb
A new strategy to improve the efficiency and sustainability of Candida parapsilosis catalyzing deracemization of (R,S)-1-phenyl-1,2-ethanediol under non-growing conditions: increase of NADPH availability.
2009 Jan
Using a water-immiscible ionic liquid to improve asymmetric reduction of 4-(trimethylsilyl)-3-butyn-2-one catalyzed by immobilized Candida parapsilosis CCTCC M203011 cells.
2009 Oct 22
[Gene cloning and expression of a novel (S)-specific carbonyl reductase].
2010 Jan
Enhancement of substrate concentration in microbial stereoinversion through one-pot oxidation and reduction by aqueous two-phase system.
2010 Mar
Improved production of (R)-1-phenyl-1,2-ethanediol by a codon-optimized R-specific carbonyl reductase from Candida parapsilosis in Escherichia coli.
2010 Mar
Highly enantioselective reduction of 2-hydroxy-1-phenylethanone to enantiopure (R)-phenyl-1,2-ethanediol using Saccharomyces cerevisiae of remarkable reaction stability.
2010 Nov
Enhancement of Candida parapsilosis catalyzing deracemization of (R,S)-1-phenyl-1,2-ethanediol to its (S)-enantiomer by a highly productive "two-in-one" resin-based in situ product removal strategy.
2010 Nov
Biotransformation of α-bromoacetophenones by the marine fungus Aspergillus sydowii.
2010 Oct
Characterization of the epoxide hydrolase NcsF2 from the neocarzinostatin biosynthetic gene cluster.
2010 Sep 3
Modification of the metabolism and toxicity of styrene and styrene oxide in hepatic cytochrome P450 reductase deficient mice and CYP2F2 deficient mice.
2012 Apr 11
Metabolism of styrene to styrene oxide and vinylphenols in cytochrome P450 2F2- and P450 2E1-knockout mouse liver and lung microsomes.
2014 Jan 21
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 09:05:42 GMT 2023
Edited
by admin
on Sat Dec 16 09:05:42 GMT 2023
Record UNII
2ZAC511UK8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
STYRENE GLYCOL
MI  
Common Name English
NSC-406601
Code English
PHENYL GLYCOL
Common Name English
1-PHENYL-1,2-ETHANEDIOL
Systematic Name English
1,2-ETHANEDIOL, 1-PHENYL-
Systematic Name English
STYRENE GLYCOL [MI]
Common Name English
1,2-DIHYDROXY-2-PHENYLETHANE
Systematic Name English
(±)-STYRENE GLYCOL
Common Name English
1-PHENYLETHYLENE GLYCOL
Systematic Name English
1,2-DIHYDROXY-1-PHENYLETHANE
Systematic Name English
STYRENE GLYCOL, (±)-
Common Name English
PHENYLETHYLENE GLYCOL
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
202-258-1
Created by admin on Sat Dec 16 09:05:42 GMT 2023 , Edited by admin on Sat Dec 16 09:05:42 GMT 2023
PRIMARY
PUBCHEM
7149
Created by admin on Sat Dec 16 09:05:42 GMT 2023 , Edited by admin on Sat Dec 16 09:05:42 GMT 2023
PRIMARY
EPA CompTox
DTXSID8042422
Created by admin on Sat Dec 16 09:05:42 GMT 2023 , Edited by admin on Sat Dec 16 09:05:42 GMT 2023
PRIMARY
NSC
406601
Created by admin on Sat Dec 16 09:05:42 GMT 2023 , Edited by admin on Sat Dec 16 09:05:42 GMT 2023
PRIMARY
FDA UNII
2ZAC511UK8
Created by admin on Sat Dec 16 09:05:42 GMT 2023 , Edited by admin on Sat Dec 16 09:05:42 GMT 2023
PRIMARY
MERCK INDEX
m10261
Created by admin on Sat Dec 16 09:05:42 GMT 2023 , Edited by admin on Sat Dec 16 09:05:42 GMT 2023
PRIMARY Merck Index
CAS
93-56-1
Created by admin on Sat Dec 16 09:05:42 GMT 2023 , Edited by admin on Sat Dec 16 09:05:42 GMT 2023
PRIMARY