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302155

(S)-(+)-1-Phenyl-1,2-ethanediol

Name: (<I>S</I>)-(+)-1-Phenyl-1,2-ethanediol
Brand: ALDRICH

99%

Sinonimo/i:

(+)-Styrene glycol, (S)-(+)-Phenylethylene glycol

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About This Item

Formula condensata:

HOCH₂CH(C₆H₅)OH

Numero CAS:

25779-13-9

Peso molecolare:

138.16

Beilstein:

3196197

Numero MDL:

MFCD00066256

Codice UNSPSC:

12352002

ID PubChem:

24858237

NACRES:

NA.22

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Sigma-Aldrich

256269

(S,S)-(−)-Hydrobenzoin

Saggio

99%

Attività ottica

[α]18/D +66°, c = 1 in chloroform

Punto di fusione

64-67 °C (lit.)

Gruppo funzionale

hydroxyl
phenyl

Stringa SMILE

OC[C@@H](O)c1ccccc1

InChI

1S/C8H10O2/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8-10H,6H2/t8-/m1/s1
PWMWNFMRSKOCEY-MRVPVSSYSA-N

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Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

320.0 °F - closed cup

Punto d’infiammabilità (°C)

160.00 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Simultaneous determination of phenylglyoxylic acid, mandelic acid, styrene glycol and hippuric acid in primary culture of rat hepatocytes incubate by high-performance liquid chromatography.

Jin-Zhao Wang et al.

Biomedical chromatography : BMC, 21(5), 497-501 (2007-03-16)

A simple HPLC method for the simultaneous determination of phenylglyoxylic acid (PGA), mandelic acid (MA), styrene glycol (SG) and hippuric acid (HA) in cell culture medium was developed. Analysis was performed on a C(18) column with a mobile phase composed

[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].

Rongzhen Zhang et al.

Wei sheng wu xue bao = Acta microbiologica Sinica, 49(2), 204-209 (2009-05-19)

To prepare (S)-1-phenyl-1,2-ethanediol by a one-step method, we constructed an enzyme coupled system consisting of (R)- and (S)-specific carbonyl reductases in Escherichia coli. The genes coding (R)- and (S)-specific carbonyl reductases from Candida parapsilosis were inserted into a co-expression vector

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.

Li Cao et al.

Biotechnology and bioengineering, 94(3), 522-529 (2006-02-25)

Soluble epoxide hydrolase (EH) from the potato Solanum tuberosum and an evolved EH of the bacterium Agrobacterium radiobacter AD1, EchA-I219F, were purified for the enantioconvergent hydrolysis of racemic styrene oxide into the single product (R)-1-phenyl-1,2-ethanediol, which is an important intermediate

Block copolymers of ethylene oxide and phenyl glycidyl ether: micellization, gelation, and drug solubilization.

Pablo Taboada et al.

Langmuir : the ACS journal of surfaces and colloids, 21(12), 5263-5271 (2005-06-01)

Three triblock copolymers of ethylene oxide and phenyl glycidyl ether, type E(m)G(n)E(m), where G = OCH2CH(CH2OC6H5) and E = OCH2CH2, were synthesized and characterized by gel-permeation chromatography, matrix-assisted laser desorption ionization time-of-flight mass spectrometry, and NMR spectroscopy. Their association properties

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.

Qingsen Hu et al.

Bioresource technology, 101(21), 8461-8463 (2010-06-25)

In this study, a highly efficient process for Candida parapsilosis-catalyzed deracemization of racemic 1-phenyl-1,2-ethanediol (PED) was described, based on a resin-based in situ substrate feeding and product removal (ISSFPR) methodology. The resin H103 was selected and used to keep the

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