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butyl (R)-2-chloropropionate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79398-16-6

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79398-16-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79398-16-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,9 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79398-16:
(7*7)+(6*9)+(5*3)+(4*9)+(3*8)+(2*1)+(1*6)=186
186 % 10 = 6
So 79398-16-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H13ClO2/c1-3-4-5-10-7(9)6(2)8/h6H,3-5H2,1-2H3/t6-/m1/s1

79398-16-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name butyl (R)-2-chloropropanoate

1.2 Other means of identification

Product number -
Other names -

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:79398-16-6 SDS

79398-16-6Downstream Products

79398-16-6Relevant academic research and scientific papers

Superparamagnetic nanoparticle-supported enzymatic resolution of racemic carboxylates

Gardimalla, Hari M. R.,Mandal, Deendayal,Stevens, Philip D.,Yen, Max,Gao, Yong

, p. 4432 - 4434 (2007/10/03)

Candida rugosa lipase immobilized on maghemite nanoparticles demonstrated high stereoselectivity in kinetic resolution of racemic carboxylates and improved long-term stability over its parent free enzyme, allowing the supported enzyme to be repeatedly used for a series of chiral resolution reactions. The Royal Society of Chemistry 2005.

Resolution of Racemic Mixtures via Lipase Catalysis in Organic Solvents

Kirchner, Gerald,Scollar, Mark P.,Klibanov, Alexander M.

, p. 7072 - 7076 (2007/10/02)

Yeast lipase and porcine pancreatic lipase have been found to vigorously function in nearly anhydrous organic solvents and catalyze the reactions of esterification and transesterification, respectively, in highly stereoselective manner.With use of these enzymatic processes, a number of optically active alcohols, carboxylic acids, and their esters have been prepared on a gram scale.

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