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Benzeneacetic acid, a-hydroxy-, cyclohexyl ester, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61597-97-5

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61597-97-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61597-97-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,9 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61597-97:
(7*6)+(6*1)+(5*5)+(4*9)+(3*7)+(2*9)+(1*7)=155
155 % 10 = 5
So 61597-97-5 is a valid CAS Registry Number.

61597-97-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-cyclohexyl mandelate

1.2 Other means of identification

Product number -
Other names (S)-Hydroxy-phenyl-acetic acid cyclohexyl ester

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:61597-97-5 SDS

61597-97-5Downstream Products

61597-97-5Relevant academic research and scientific papers

Chiral N,N′-dioxide-FeCl3 complex-catalyzed asymmetric intramolecular Cannizzaro reaction

Wu, Wangbin,Liu, Xiaohua,Zhang, Yuheng,Ji, Jie,Huang, Tianyu,Lin, Lili,Feng, Xiaoming

supporting information, p. 11646 - 11649 (2015/07/15)

An environmentally benign catalyst, the N,N′-dioxide-FeCl3 complex, has been developed for the asymmetric intramolecular Cannizzaro reaction. Aryl and alkyl glyoxal monohydrates were applied to obtain α-hydroxy acid esters with excellent results. Deuterium-label and control experiments shed light on the reaction mechanism.

Study of enantioselective hydrogenation of bulky esters of phenylglyoxylic acid on Pt-CD and Pt-β-ICN chiral catalysts: Steric effect of ester groups and inversion of enantioselectivity

Szori, Kornél,Balázsik, Katalin,Felf?ldi, Károly,Bartók, Mihály

, p. 149 - 154 (2007/10/03)

Enantioselective hydrogenation of seven different esters of phenylglyoxylic acid was investigated by variation of the bulkiness at ester side of the substrates [Ph{single bond}C(O){single bond}C(O)OR, R = Me (l), cyclohexyl (2), adamantyl (3), cis-decahyd

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