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62173-99-3

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62173-99-3 Usage

Uses

Benzyl (S)-(+)-mandelate can be used as a reactant to prepare: α-Hydroxy-N-(2-phenylethyl)benzenepropanamide by reacting with benzeneethanamine. Benzyl-2-fluoro-2-phenylacetate by deoxyfluorination of alcohols.

Check Digit Verification of cas no

The CAS Registry Mumber 62173-99-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,7 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 62173-99:
(7*6)+(6*2)+(5*1)+(4*7)+(3*3)+(2*9)+(1*9)=123
123 % 10 = 3
So 62173-99-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H14O3/c16-14(13-9-5-2-6-10-13)15(17)18-11-12-7-3-1-4-8-12/h1-10,14,16H,11H2/t14-/m0/s1

62173-99-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Packaging
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  • TCI America

  • (M1355)  Benzyl L-(+)-Mandelate  >98.0%(GC)

  • 62173-99-3

  • 5g

  • 430.00CNY

  • Detail
  • TCI America

  • (M1355)  Benzyl L-(+)-Mandelate  >98.0%(GC)

  • 62173-99-3

  • 25g

  • 1,690.00CNY

  • Detail
  • Aldrich

  • (458295)  Benzyl(S)-(+)-mandelate  99%

  • 62173-99-3

  • 458295-5G

  • 409.50CNY

  • Detail

62173-99-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name L-(+)-MANDELIC ACID BENZYL ESTER

1.2 Other means of identification

Product number -
Other names benzyl (2S)-2-hydroxy-2-phenylacetate

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:62173-99-3 SDS

62173-99-3Relevant articles and documents

Shepard,Stevens

, p. 951 (1971)

Cobalt-Catalyzed Transfer Hydrogenation of α-Ketoesters and N-Cyclicsulfonylimides Using H2O as Hydrogen Source

Gao, Yang,Zhang, Xuexin,Laishram, Ronibala Devi,Chen, Jingchao,Li, Kangkui,Zhang, Keyang,Zeng, Guangzhi,Fan, Baomin

, p. 3991 - 3997 (2019/08/02)

A Co-catalyzed effective transfer hydrogenation of various α-ketoesters and N-cyclicsulfonylimides by safe and environmentally benign H2O as hydrogen source is described. The reaction used easily available and easy to handle zinc metal as a reductant. Interestingly, the catalytic system does not require ligand for reduction of N-cyclicsulfonylimides. (Figure presented.).

Boron-Catalyzed O-H Bond Insertion of α-Aryl α-Diazoesters in Water

San, Htet Htet,Wang, Shi-Jun,Jiang, Min,Tang, Xiang-Ying

, p. 4672 - 4676 (2018/08/09)

A catalytic, metal-free O-H bond insertion of α-diazoesters in water in the presence of B(C6F5)3·nH2O (2 mol %) was developed, affording a series of α-hydroxyesters in good to excellent yields. The reaction features easy operation and wide substrate scope, and importantly, no metal is needed as compared with the conventional methods. Significantly, this approach further expands the applications of B(C6F5)3 under water-tolerant conditions.

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