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butyl 2,3-dichloropropionate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72726-18-2

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72726-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72726-18-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,7,2 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 72726-18:
(7*7)+(6*2)+(5*7)+(4*2)+(3*6)+(2*1)+(1*8)=132
132 % 10 = 2
So 72726-18-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H12Cl2O2/c1-2-3-4-11-7(10)6(9)5-8/h6H,2-5H2,1H3

72726-18-2SDS

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 butyl 2,3-dichloropropanoate

1.2 Other means of identification

Product number -
Other names n-Butyl 2,3-dichloropropionate

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:72726-18-2 SDS

72726-18-2Downstream Products

72726-18-2Relevant academic research and scientific papers

Single-isomer iodochlorination of alkynes and chlorination of alkenes using tetrabutylammonium iodide and dichloroethane

Ho, Michael L.,Flynn, Alison B.,Ogilvie, William W.

, p. 977 - 983 (2007/10/03)

(Chemical Equation Presented) The efficient formation of single-isomer, differentially halogenated alkenes and alkanes is described. These structures were generated by treatment of the appropriate alkyne or alkene with tetrabutylammonium iodide in refluxing dichloroethane. This process is highly selective as evidenced by control experiments using ICl. Treatment of the same alkenes and alkynes directly with iodine monochloride resulted in complex, inseparable mixtures of regio- and stereoisomers. Mechanistic studies indicated that the Bu4NI reaction most likely proceeded through the slow generation of ICl. Complexation of ICl with Bu4NI is also a key controlling element that leads to perfect regio-, chemo-, and stereoselectivity in these processes.

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