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(S)-(+)-1-Phenyl-1,2-ethanediol is a white to light yellow crystalline powder that is an extremely valuable and versatile alcohol. It is characterized by its chiral structure, which makes it a crucial component in various applications across different industries.

25779-13-9

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25779-13-9 Usage

Uses

Used in Pharmaceutical Industry:
(S)-(+)-1-Phenyl-1,2-ethanediol is used as a chiral building block in organic synthesis for the preparation of chiral 2-amino-1-phenylethanols. These chiral 2-amino-1-phenylethanols serve as pharmaceutical intermediates, which are essential in the development of various drugs and medications.
Used in Organic Synthesis:
(S)-(+)-1-Phenyl-1,2-ethanediol is also used as a chiral building block in the field of organic synthesis. Its unique chiral structure allows for the creation of a wide range of compounds with specific properties, making it an indispensable tool in the synthesis of complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 25779-13-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,7,7 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 25779-13:
(7*2)+(6*5)+(5*7)+(4*7)+(3*9)+(2*1)+(1*3)=139
139 % 10 = 9
So 25779-13-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H10O2/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8-10H,6H2/t8-/m1/s1

25779-13-9 Well-known Company Product Price

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  • TCI America

  • (P1151)  (S)-(+)-1-Phenylethane-1,2-diol  >98.0%(GC)

  • 25779-13-9

  • 1g

  • 390.00CNY

  • Detail
  • TCI America

  • (P1151)  (S)-(+)-1-Phenylethane-1,2-diol  >98.0%(GC)

  • 25779-13-9

  • 5g

  • 1,250.00CNY

  • Detail
  • Alfa Aesar

  • (L09836)  (S)-(+)-Phenyl-1,2-ethanediol, 97%   

  • 25779-13-9

  • 250mg

  • 125.0CNY

  • Detail
  • Alfa Aesar

  • (L09836)  (S)-(+)-Phenyl-1,2-ethanediol, 97%   

  • 25779-13-9

  • 1g

  • 337.0CNY

  • Detail
  • Sigma-Aldrich

  • (77845)  (S)-(+)-1-Phenyl-1,2-ethanediol  purum, ≥98.0% (sum of enantiomers, HPLC)

  • 25779-13-9

  • 77845-5G

  • 4,124.25CNY

  • Detail
  • Aldrich

  • (302155)  (S)-(+)-1-Phenyl-1,2-ethanediol  99%

  • 25779-13-9

  • 302155-1G

  • 873.99CNY

  • Detail

25779-13-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S)-1-phenylethane-1,2-diol

1.2 Other means of identification

Product number -
Other names (S)-(+)-Styreneglycol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:25779-13-9 SDS

25779-13-9Relevant academic research and scientific papers

Marked improvement in the asymmetric reduction of 2-hydroxyacetophenone with mut-AcCR in a biphasic system

Chao, Peng,Li, Dong-Li,Lou, Wen-Yong,Wang, Yao-Ying,Wei, Ping,Zong, Min-Hua,Zou, Qing-Jian

, (2020)

(S)-1-Phenyl-1,2-ethanediol (PED) is a vital chiral block in specialty chemical industries. The biotransformation of 2-hydroxyacetophenone (2-HAP) to (S)-PED was conducted successfully catalyzed with BL21(DE3)(pETDuet-gst-mut-accr-gdh) which harboring a c

Enantioselective catalysis using planar chiral η6-arene chromium complexes: 1,2-Diols as cycloaddition catalysts

Jones, Graham B.,Guzel, Mustafa,Heaton, Steven B.

, p. 4303 - 4320 (2000)

A highly selective Diels-Alder catalyst has been prepared from a commercially available tetrahydronaphthalene diol. Stereocontrol is greatly enhanced by introduction of a planar chiral arene chromium tricarbonyl group, achieved by face selective complexat

Coexpression of a carbonyl reductase and glucose 6-phosphate dehydrogenase in Pichia pastoris improves the production of (S)-1-phenyl-1,2-ethanediol

Geng, Yawei,Zhang, Rongzhen,Xu, Yan,Wang, Shanshan,Sha, Chong,Xiao, Rong

, p. 172 - 178 (2011)

To develop an efficient biocatalyst to produce optically active (S)-phenyl ethanediol (PED), a carbonyl reductase SCRII and glucose 6-phosphate dehydrogenase were coexpressed intracellularly in Pichia pastoris. The recombinant enzyme PpSCRII was purified

Method for synthesizing chiral 1,2-diol compound

-

Paragraph 0085-0093, (2021/07/21)

The invention relates to a method for synthesizing a chiral 1,2-diol compound, which comprises the following steps: sequentially adding a cobalt catalyst, a ligand, alpha-hydroxy ketone, an organic solvent and silane into a reaction system at 20-30 DEG C in a nitrogen atmosphere, then stirring the mixture, and carrying out column chromatography separation on the obtained product to obtain the chiral 1,2-diol compound. The high-yield cobalt catalyst in the earth crust is used, meanwhile, cheap silane (PMHS, 500 g/298 yuan) is used as a reducing agent, the asymmetric reduction reaction of alpha-hydroxy ketone can be efficiently achieved under the mild condition, and the chiral 1,2-diol compound with high yield and optical activity is obtained. Moreover, through the creative labor of the inventor, the reaction yield can reach 99%, and meanwhile, the content of the target product in the generated reaction product is 99% (namely, the yield is 99%, 99% ee).

Tridentate nitrogen phosphine ligand containing arylamine NH as well as preparation method and application thereof

-

Paragraph 0117-0120, (2021/06/26)

The invention discloses a tridentate nitrogen phosphine ligand containing arylamine NH as well as a preparation method and application thereof, and belongs to the technical field of organic synthesis. The tridentate nitrogen phosphine ligand disclosed by the invention is the first case of tridentate nitrogen phosphine ligand containing not only a quinoline amine structure but also chiral ferrocene at present, a noble metal complex of the type of ligand shows good selectivity and extremely high catalytic activity in an asymmetric hydrogenation reaction, meanwhile, a cheap metal complex of the ligand can also show good selectivity and catalytic activity in the asymmetric hydrogenation reaction, and is very easy to modify in the aspects of electronic effect and space structure, so that the ligand has huge potential application value. A catalyst formed by the ligand and a transition metal complex can be used for catalyzing various reactions, can be used for synthesizing various drugs, and has important industrial application value.

Reprogramming Epoxide Hydrolase to Improve Enantioconvergence in Hydrolysis of Styrene Oxide Scaffolds

Li, Fu-Long,Qiu, Yan-Yan,Zheng, Yu-Cong,Chen, Fei-Fei,Kong, Xu–Dong,Xu, Jian-He,Yu, Hui-Lei

supporting information, p. 4699 - 4706 (2020/09/21)

Enantioconvergent hydrolysis by epoxide hydrolase is a promising method for the synthesis of important vicinal diols. However, the poor regioselectivity of the naturally occurring enzymes results in low enantioconvergence in the enzymatic hydrolysis of styrene oxides. Herein, modulated residue No. 263 was redesigned based on structural information and a smart variant library was constructed by site-directed modification using an “optimized amino acid alphabet” to improve the regioselectivity of epoxide hydrolase from Vigna radiata (VrEH2). The regioselectivity coefficient (r) of variant M263Q for the R-isomer of meta-substituted styrene oxides was improved 40–63-fold, and variant M263V also exhibited higher regioselectivity towards the R-isomer of para-substituted styrene oxides compared with the wild type, which resulted in improved enantioconvergence in hydrolysis of styrene oxide scaffolds. Structural insight showed the crucial role of residue No. 263 in modulating the substrate binding conformation by altering the binding surroundings. Furthermore, increased differences in the attacking distance between nucleophilic residue Asp101 and the two carbon atoms of the epoxide ring provided evidence for improved regioselectivity. Several high-value vicinal diols were readily synthesized (>88% yield, 90%–98% ee) by enantioconvergent hydrolysis using the reprogrammed variants. These findings provide a successful strategy for enhancing the enantioconvergence of native epoxide hydrolases through key single-site mutation and more powerful enzyme tools for the enantioconvergent hydrolysis of styrene oxide scaffolds into single (R)-enantiomers of chiral vicinal diols. (Figure presented.).

Enantiocomplementary C–H Bond Hydroxylation Combining Photo-Catalysis and Whole-Cell Biocatalysis in a One-Pot Cascade Process

Peng, Yongzhen,Li, Danyang,Fan, Jiajie,Xu, Weihua,Xu, Jian,Yu, Huilei,Lin, Xianfu,Wu, Qi

supporting information, p. 821 - 825 (2020/02/20)

Enantiocomplementary hydroxylation of alkyl aromatics through a one-pot photo-biocatalytic cascade reaction is described. The photoredox process is implemented in aqueous phase with O2 as oxidant and the subsequent (R)- or (S)-selective bioreduction is performed by whole cell system without the addition of the expensive cofactor (NADPH). This mild, operationally simple protocol transforms a wide variety of readily available aromatic compounds into valuable chiral alcohols with high yield (up to 90 %) and stereoselectivity (up to 99 %), thereby displaying important potentials in organic synthesis.

Application of the redox system of Nocardia corallina B-276 in the enantioselective biotransformation of ketones and alcohols

Alvarez, Norberto Manjarrez,Pérez Méndez, Herminia I.,Oba, Aida Solís,Cabello, Lucía Ortega,Lara Carvajal, María T.,Valencia Ledezma, Omar E.,Martínez-Casares, Rubria M.

, p. 279 - 290 (2020/06/01)

The aim of this research was to evaluate the redox system of Nocardia corallina B-276 in the biotransformation of 1-phenyl-1-propanone (1a), 2-hydroxy-1-phenylethanone (2a) and methyl (2-chlorophenyl)(oxo)acetate (3a) into 1-phenylpropan-1-ol (1b), 1-phenyl-1,2-ethanediol (2b) and methyl (2-chlorophenyl)(hydroxy)acetate (3b). The biomass of N. corallina was obtained in a liquid medium with an initial pH of 8.50, but the pH changed during the 96 h of the culture media, the final pH was between 4.74 and 7.62. The N. corallina biomass biocatalyzed the enantioselective reduction of 1a–3a to the corresponding alcohols. Whereas, during the process of oxidation of the rac-alcohols 1b–3b, 1b was oxidized in enantioselective way, the oxidation of 2b was not selective, but 3b was biotransformed mainly to (R)-3b. These results are indicative that N. corallina produced reductases and oxidases, whereby the biocatalytic activity was influenced by the final pH of the culture media, the reaction time and structure of the substrate.

Highly regio- and enantio-selective hydrolysis of two racemic epoxides by GmEH3, a novel epoxide hydrolase from Glycine max

Zhang, Chen,Li, Chuang,Zhu, Xiu-xiu,Liu, You-yi,Zhao, Jun,Wu, Min-chen

, p. 2795 - 2803 (2020/09/01)

A novel epoxide hydrolase from Glycine max, designated GmEH3, was excavated based on the computer-aided analysis. Then, gmeh3, a GmEH3-encoding gene, was cloned and successfully expressed in E. coli Rosetta(DE3). Among the ten investigated rac-epoxides, GmEH3 possessed the highest and best complementary regioselectivities (regioselectivity coefficients, αS = 93.7% and βR = 97.2%) in the asymmetric hydrolysis of rac-m-chlorostyrene oxide (5a), and the highest enantioselectivity (enantiomeric ratio, E = 55.6) towards rac-phenyl glycidyl ether (7a). The catalytic efficiency (kcatS/KmS = 2.50 mM?1 s?1) of purified GmEH3 for (S)-5a was slightly higher than that (kcatR/KmR = 1.52 mM?1 s?1) for (R)-5a, whereas the kcat/Km (5.16 mM?1 s?1) for (S)-7a was much higher than that (0.09 mM?1 s?1) for (R)-7a. Using 200 mg/mL wet cells of E. coli/gmeh3 as the biocatalyst, the scale-up enantioconvergent hydrolysis of 150 mM rac-5a at 25 °C for 1.5 h afforded (R)-5b with 90.2% eep and 95.4% yieldp, while the kinetic resolution of 500 mM rac-7a for 2.5 h retained (R)-7a with over 99% ees and 43.2% yields. Furthermore, the sources of high regiocomplementarity of GmEH3 for (S)- and (R)-5a as well as high enantioselectivity towards rac-7a were analyzed via molecular docking (MD) simulation.

Absolute stereochemical determination of 1,2-diols via complexation with dinaphthyl borinic acid

Torabi Kohlbouni, Saeedeh,Sarkar, Aritra,Zhang, Jun,Li, Xiaoyong,Borhan, Babak

supporting information, p. 817 - 823 (2020/03/26)

Rapid derivatization of chiral 1,2-diols with dinaphthyl borinic acid (DBA) leads to a cyclic boronate, enabling the absolute stereochemical prediction via exciton-coupled circular dichroic (ECCD) of the naphthyl groups. Aryl- and alkyl-substituted 1,2-diols derivatized with DBA yield a predictable ECCD, which is also in agreement with theoretical predictions derived from computationally minimized structures.

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