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77666-53-6

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77666-53-6 Usage

Class of organic compounds

Oxadiazoles

Heterocycle

Contains an oxadiazole ring

Nitrogen atoms positions

1 and 2

Oxygen atom position

5

Derivative

Contains a methyl group at position 3

Derivative

Contains a nitro group at position 4

Common use

Synthesis of pharmaceuticals, agrochemicals, and specialty chemicals

Unique structure

Contributes to its applications in various fields

Potential applications

Medicine, materials science, and agriculture

Check Digit Verification of cas no

The CAS Registry Mumber 77666-53-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,6,6 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 77666-53:
(7*7)+(6*7)+(5*6)+(4*6)+(3*6)+(2*5)+(1*3)=176
176 % 10 = 6
So 77666-53-6 is a valid CAS Registry Number.

77666-53-6SDS

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 3-Methyl-4-nitro-1,2,5-oxadiazole

1.2 Other means of identification

Product number -
Other names furazan,methylnitro

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:77666-53-6 SDS

77666-53-6Upstream product

77666-53-6Relevant articles and documents

3-alkyl-4-nitrofurazans – plasticizers for polymers

Lotmentsev, Yury M.,Kondakova, Natalya N.,Bakeshko, Artem V.,Kozeev, Andrei M.,Sheremetev, Aleksei B.

, p. 740 - 745 (2017)

Oxidation of 4-alkylfurazan-3-amines to the corresponding nitrofurazans was achieved using mixtures of hydrogen peroxide. The volatility of the products as a function of the size of substituent R, has been studied. The phase and relaxation transitions were characterized and the thermodynamic compatibility with polyester urethane was established. The melting points and melting enthalpies of alkylnitrofurazans were determined.

Reactions of 3-amino-4-methylfurazan with nitrating agents

Sheremetev,Aleksandrova

, p. 1715 - 1719 (2007/10/03)

Depending on the type of nitrating agent and the reaction temperature, nitration of 3-amino-4-methylfurazan 1 gives either nitramine or the products of formal oxidation of the amino group, namely, nitroso-, nitro-, azo-, and azoxyfurazans. The methyl group of compound 1 is resistant against all the nitrating agents studied.

THE SYNTHESIS OF 3-NITROSO-4-R-FURAZANES

Sheremetev, A. B.,Novikova, T. S.,Mel'nikova, T. M.,Khmel'nitskii, L. I.

, p. 1073 (2007/10/02)

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