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1,2,5-Oxadiazole, 3-nitro-4-(3,4,5-trinitrophenyl)-, 5-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

177788-45-3

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177788-45-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 177788-45-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,7,8 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 177788-45:
(8*1)+(7*7)+(6*7)+(5*7)+(4*8)+(3*8)+(2*4)+(1*5)=203
203 % 10 = 3
So 177788-45-3 is a valid CAS Registry Number.

177788-45-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-nitro-2-oxido-3-(3,4,5-trinitrophenyl)-1,2,5-oxadiazol-2-ium

1.2 Other means of identification

Product number -
Other names -

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:177788-45-3 SDS

177788-45-3Downstream Products

177788-45-3Relevant academic research and scientific papers

Nitrosation of salts of 1-hydroxyimino-2,2-dinitro-1-R-ethanes, a novel method for the preparation of isomeric 3(4)-nitro-4(3)-R-furoxans

Ovchinnikov,Finogenov,Epishina,Kulikov,Strelenko,Makhova

, p. 2137 - 2146 (2011/01/09)

A novel general method for the synthesis of isomeric 3(4)-nitro-4(3)-R- furoxans is developed. 3-Nitro isomers were obtained by reaction of hydroximoyl chlorides with dinitromethane sodium salt followed by conversion of the resulting 1-substituted 1-hydroxyimino-2,2-dinitroethanes into dipotassium (or disodium salts) and their subsequent nitrosation with NaNO2 in AcOH or with N2O4. Thermal isomerization of 3-nitro isomers afforded 4-nitro isomers were prepared in high yields.

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