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2-Thiazolecarboxylicacid,4,5-dichloro-,ethylester(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79807-38-8

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79807-38-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79807-38-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,8,0 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 79807-38:
(7*7)+(6*9)+(5*8)+(4*0)+(3*7)+(2*3)+(1*8)=178
178 % 10 = 8
So 79807-38-8 is a valid CAS Registry Number.

79807-38-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4,5-dichloro-1,3-thiazole-2-carboxylate

1.2 Other means of identification

Product number -
Other names 2-thiazolecarboxylic acid,4,5-dichloro-,ethyl 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:79807-38-8 SDS

79807-38-8Upstream product

79807-38-8Downstream Products

79807-38-8Relevant academic research and scientific papers

Removal of Toluene-p-sulphonyl Groups from Sulphonamides. Part 5. Reactions of Phenylglyoxal Imines and some Tosylimines

McKay, William R.,Proctor, George R.

, p. 2443 - 2450 (2007/10/02)

Phenylglyoxal anil monomers have been shown to react with several nucleophilic reagents and the structures of the products have been elucidated.Various N-tosylarylimines also react with nucleophiles to give useful products.Phenacylimidates underwent cycloadditions with diphenylketen; such reactions gave complex results with phenacylimines, but the latter reacted with conjugated dienes in the presence of BF3 to give cycloaddition products in good yield.

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