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3-Amino-N-hydroxy-pyrazinecarboximidamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76952-35-7

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76952-35-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76952-35-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,9,5 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76952-35:
(7*7)+(6*6)+(5*9)+(4*5)+(3*2)+(2*3)+(1*5)=167
167 % 10 = 7
So 76952-35-7 is a valid CAS Registry Number.

76952-35-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Amino-N-hydroxy-2-pyrazinecarboximidamide

1.2 Other means of identification

Product number -
Other names 3-aminopyrazinecarbonitrile

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:76952-35-7 SDS

76952-35-7Relevant academic research and scientific papers

Construction of Bicyclic 1,2,3-Triazine N-Oxides from Aminocyanides

Liu, Yuji,Qi, Xiujuan,Zhang, Wenquan,Yin, Ping,Cai, Ziwu,Zhang, Qinghua

supporting information, p. 734 - 738 (2021/01/09)

Using a facile and cost-effective method, nine bicyclic 1,2,3-triazine 2-oxides were synthesized from o-aminocyanide substrates through an unusual nitration cyclization. The reaction mechanism was studied experimentally and theoretically. Moreover, nine 1

RING TRANSFORMATIONS OF SOME 4-AMINOPTERIDINE 3-OXIDES AND DERIVATIVES

Kocevar, Marjan,Stanovnik, Branko,Tisler, Miha

, p. 823 - 829 (2007/10/02)

Syntheses of 4-aminopteridine 3-oxides are described.The pyrimidine part undergoes transformations with various reagents to give 4-hydroxyaminopteridines, substituted pyrazines, or substituted 1,2,4-oxadiazolylpyrazines. s-Triazolo(1,5-a)pyrazines can be prepared from 1,2,4-oxadiazolylpyrazines.The ring opening of the pyrimidine part of pteridines proceeds either py a C2-N3 or N3-C4 bond cleavage.

Syntheses and Transformations of Some 1,2,4-Oxadiazolylpyrazines

Kocevar, M.,Stanovnik, B.,Tisler, M.

, p. 1397 - 1402 (2007/10/02)

Cyanopyrazines with an ortho-amino, oxo and other groups are transformed into the corresponding amidoximes.From these the corresponding 1,2,4-oxadiazolyl derivatives can be prepared and interconversions to the corresponding pteridine 3-oxides are described.

SOME NEW SYNTHETIC APPROACHES FOR THE PREPARATION OF PTERIDINE-3-OXIDES AND PTERIDINES

Kocevar, Marjan,Stanovnik, Branko,Tisler, Miha

, p. 293 - 296 (2007/10/02)

Starting from 2-amino-3-cyanopyrazine some new syntheses of 4-substituted pteridines and pteridine-3-oxides have been devised.

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