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1H-4,1,2-Benzothiadiazine-3-carboxylic acid, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62225-55-2

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62225-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62225-55-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,2 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62225-55:
(7*6)+(6*2)+(5*2)+(4*2)+(3*5)+(2*5)+(1*5)=102
102 % 10 = 2
So 62225-55-2 is a valid CAS Registry Number.

62225-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1H-4,1,2-benzothiadiazine-3-carboxylate

1.2 Other means of identification

Product number -
Other names 1H-4,1,2-Benzothiadiazine-3-carboxylic acid,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:62225-55-2 SDS

62225-55-2Upstream product

62225-55-2Downstream Products

62225-55-2Relevant academic research and scientific papers

Intramolecular Cyclisations of Nitrile Imines bearing a Thioether Function

Bruche, Luca,Garanti, Luisa,Zecchi, Gaetano

, p. 2245 - 2249 (1981)

N-Aryl nitrile imines bearing a thioether function in the ortho-position were generated in situ on treating the corresponding hydrazonyl chlorides with triethylamine in boiling benzene.In all cases, the major products were 4,1,2-benzothiadiazines arising from intramolecular participarion of the sulphur and subsequent evolution of transient cyclic ylides.Minor products due to an intramolecular 1,3-dipolar cycloaddition were sometimes obtained.

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