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73332-79-3

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73332-79-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73332-79-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,3,3 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73332-79:
(7*7)+(6*3)+(5*3)+(4*3)+(3*2)+(2*7)+(1*9)=123
123 % 10 = 3
So 73332-79-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H7N3O3/c1-4-3-8-5(9(10)11)2-7-6(8)12-4/h2,4H,3H2,1H3

73332-79-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-5-nitro-2,3-dihydroimidazo[2,1-b][1,3]oxazole

1.2 Other means of identification

Product number -
Other names 2-methyl-5-nitro-2,3-dihydro-imidazo[2,1-b]oxazole

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:73332-79-3 SDS

73332-79-3Downstream Products

73332-79-3Relevant articles and documents

Nitroimidazoles XXI 2,3-dihydro-6-nitroimidazo[2,1-b]oxazoles with antitubercular activity

Nagarajan,Shankar,Rajappa,Shenoy,Costa-Pereira

, p. 631 - 633 (2007/10/02)

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Potential Radiosensitizing Agents. 2. Synthesis and Biological Activity of Derivatives of Dinitroimidazole with Oxiranes

Sehgal, Raj K.,Webb, Matthew W.,Agrawal, Krishna C.

, p. 601 - 604 (2007/10/02)

A series of 1-substituted 2,4-dinitroimidazole analogues have been synthesized and tested for their radiosensitizing ability for selectively sensitizing hypoxic mammalian cells to the lethal effect of radiation.The reaction of 2,4(5)-dinitroimidazole (1) with a variety of oxiranes upon heating in absolute ethanol yielded the expected 1-substituted 2,4-dinitroimidazoles (2) and also resulted in the formation of a novel class of isomeric nitroimidazooxazoles (3 and 4) by intramolecular cyclization.The results of radiosensitizing activity of these agents against hypoxic Chinese hamster cells (V-79) indicated that 2,4-dinitroimidazoles were better sensitizers than the nitroimidazooxazoles, suggesting the necessity of the 2-nitro function in the molecule.The 1-(2-hydroxy-3-methoxypropyl)-2,4-dinitroimidazole (2d) was found to be the most effective radiosensitizer of this series.

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