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229322-23-0

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229322-23-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 229322-23-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,9,3,2 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 229322-23:
(8*2)+(7*2)+(6*9)+(5*3)+(4*2)+(3*2)+(2*2)+(1*3)=120
120 % 10 = 0
So 229322-23-0 is a valid CAS Registry Number.

229322-23-0SDS

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 6-(hydroxymethyl)benzo[1,2-c]1,2,5-oxadiazole N1-oxide

1.2 Other means of identification

Product number -
Other names 6-(hydroxymethyl)benzo[c][1,2,5]oxadiazole 1-oxide

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:229322-23-0 SDS

229322-23-0Relevant articles and documents

PYROLLIDINE-BASED COMPOUNDS

-

Page/Page column 24, (2009/08/16)

The present invention discloses the compounds of formula ( I ) or a pharmaceutically acceptable derivative, salt or prodrug thereof, which can inhibit HIV replication.

1,2,5-Oxadiazole N-oxide derivatives and related compounds as potential antitrypanosomal drugs: Structure-activity relationships

Cerecetto, Hugo,Di Maio, Rossanna,González, Mercedes,Risso, Mercedes,Saenz, Patricia,Seoane, Gustavo,Denicola, Ana,Peluffo, Gonzalo,Quijano, Celia,Olea-Azar, Claudio

, p. 1941 - 1950 (2007/10/03)

The syntheses of a new series of derivatives of 1,2,5-oxadiazole N- oxide, benzo[1,2-c]1,2,5-oxadiazole N-oxide, and quinoxaline di-N-oxide are described. In vitro antitrypanosomal activity of these compounds was tested against epimastigote forms of Trypa

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