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2,2'-azoxymisonidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78130-16-2

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78130-16-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78130-16-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,1,3 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 78130-16:
(7*7)+(6*8)+(5*1)+(4*3)+(3*0)+(2*1)+(1*6)=122
122 % 10 = 2
So 78130-16-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H22N6O5/c1-24-9-11(21)7-18-5-3-15-13(18)17-20(23)14-16-4-6-19(14)8-12(22)10-25-2/h3-6,11-12,21-22H,7-10H2,1-2H3/b20-17-

78130-16-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-[1-(2-hydroxy-3-methoxypropyl)imidazol-2-yl]-[1-(2-hydroxy-3-methoxypropyl)imidazol-2-yl]imino-oxidoazanium

1.2 Other means of identification

Product number -
Other names 2,2'-Azoxymisonidazole

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:78130-16-2 SDS

78130-16-2Downstream Products

78130-16-2Relevant academic research and scientific papers

CHEMICAL REDUCTION OF THE RADIOSENSITIZER MISONIDAZOLE BY ZINC OR GLUCOSE

Gattavecchia, Enrico,Tonelli, Domenica

, p. 689 - 694 (2007/10/02)

Misonidazole, 1-(2-nitroimidazol-1-yl)-3-methoxypropan-2-ol, was reduced by zinc dust or glucose in alomost neutral or alkaline solutions.T.I.c. of the reduction mixtures has revealed the presence of several products.Two of them have been identified as the azo and the azoxy derivatives of misonidazole.When the reduction was carried out in alkaline solution, another reaction, competitive with the reduction, was observed.This reaction, involving the loss of the nitro group, led to two products, the former deriving from a nucleophilic substitution by OH(-) and the latter from an intramolecular displacement.This kind of denitrative process must be considered when the reduction of misonidazole is performed at basic pH.In such conditions two other reduction products have been identified and a possible reaction mechanism for their formation is suggested.

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