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32653-33-1

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32653-33-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32653-33-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,6,5 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 32653-33:
(7*3)+(6*2)+(5*6)+(4*5)+(3*3)+(2*3)+(1*3)=101
101 % 10 = 1
So 32653-33-1 is a valid CAS Registry Number.

32653-33-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name L-2-chloro-hexanoic acid ,levorotatory form

1.2 Other means of identification

Product number -
Other names L-2-Chlor-hexansaeure,linksdrehende Form

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:32653-33-1 SDS

32653-33-1Downstream Products

32653-33-1Relevant articles and documents

Asymmetric Synthesis of 2-Chloro- and 2-Bromo-alkanoic acids by Halogenation of α-D-Glucofuranose-Derived Silyl Ketene Acetals.

Angibaud, P.,Chaumette, J. L.,Desmurs, J. R.,Duhamel, L.,Ple, G.,et al.

, p. 1919 - 1932 (2007/10/03)

Optically active (S)-2-bromo- and 2-chloro-alkanoic acids 6 and 7 have been obtained via the diastereoselective halogenation of chiral silyl ketene acetals 3a-f, and subsequent saponification of the resulting crude esters.Examples characterized by e.e. values up to 95percent are reported.The diastereoface selectivity is independent of the silyl ketene acetal E/Z configuration.

Asymmetric Transformation of 2-Phenyl- and 2-Chloroalkanoic Acids via Chiral Oxazolines

Shibata, Saizo,Matsushita, Hajime,Kaneko, Hajime,Noguchi, Masao,Saburi, Masahiko,Yoshikawa, Sadao

, p. 3546 - 3551 (2007/10/02)

Asymmetric transformation of racemic 2-phenyl- and 2-chloroalkanoic acids via oxazolines into the corresponding optically active acids was investigated using (S)-phenylalaninol as a chiral auxiliary.The asymmetric transformation was performed by metalatio

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