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2-[2-(3-azabicyclo[3.2.2]non-3-yl)ethyl]-5,6-dimethoxy-1,2-benzothiazol-3(2H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71998-53-3

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71998-53-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71998-53-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,9,9 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 71998-53:
(7*7)+(6*1)+(5*9)+(4*9)+(3*8)+(2*5)+(1*3)=173
173 % 10 = 3
So 71998-53-3 is a valid CAS Registry Number.

71998-53-3SDS

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 2-[2-(3-azabicyclo[3.2.2]nonan-3-yl)ethyl]-5,6-dimethoxy-1,2-benzothiazol-3-one

1.2 Other means of identification

Product number -
Other names 1,2-Benzisothiazol-3(2H)-one,2-(2-(3-azabicyclo(3.2.2)non-3-yl)ethyl)-5,6-dimethoxy

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:71998-53-3 SDS

71998-53-3Relevant academic research and scientific papers

SYNTHESIS OF BUNTE SALTS FROM 1,2-BENZISOTHIAZOL-3-ONES AND VICE VERSA

Tyrrell, A. W. R.

, p. 1753 - 1756 (2007/10/02)

1,2-Benzisothiazol-3-ones undergo ring-opening when treated with sodium hydrogen sulphite solution, giving Bunte salts, reconversion of which to benzisothiazol-3-ones can be effected with dilute alkali.

2-Substituted benzisothiazolones

-

, (2008/06/13)

A class of 2-substituted benzisothiazolones carrying a nitrogen-containing heterocyclic ring are effective in inhibiting platelet aggregation and are therefore of value in the prophylactic and therapeutic treatment of thrombotic diseases.

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