Cas 166974-98-7,Hydrazinecarboxylic acid, 2-(2-pyridinyl)-, 1,1-dimethylethyl ester (9CI)

166974-98-7

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Basic information

Product Name: Hydrazinecarboxylic acid, 2-(2-pyridinyl)-, 1,1-dimethylethyl ester (9CI)
Synonyms: Hydrazinecarboxylic acid, 2-(2-pyridinyl)-, 1,1-dimethylethyl ester (9CI);tert-Butyl 2-(pyridin-2-yl)hydrazinecarboxylate
CAS NO:166974-98-7
Molecular Formula: C10H15N3O2
Molecular Weight: 209.245
EINECS: N/A
Product Categories: N-BOC
Mol File: 166974-98-7.mol
Article Data: 2

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Hydrazinecarboxylic acid, 2-(2-pyridinyl)-, 1,1-dimethylethyl ester (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: Hydrazinecarboxylic acid, 2-(2-pyridinyl)-, 1,1-dimethylethyl ester (9CI)(166974-98-7)
EPA Substance Registry System: Hydrazinecarboxylic acid, 2-(2-pyridinyl)-, 1,1-dimethylethyl ester (9CI)(166974-98-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 166974-98-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 166974-98-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,9,7 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 166974-98:
(8*1)+(7*6)+(6*6)+(5*9)+(4*7)+(3*4)+(2*9)+(1*8)=197
197 % 10 = 7
So 166974-98-7 is a valid CAS Registry Number.

166974-98-7Upstream product

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166974-98-7Relevant articles and documents

Novel and versatile synthesis of disubstituted 1,2-dihydro-1,2,4-triazol-3- ones

Graham, Mark A.,Bethel, Paul A.,Burgess, Jonathan,Fairley, Gary,Glossop, Steve C.,Greenwood, Ryan D. R.,Jones, Clifford D.,Lovell, Scott,Swallow, Steve

, p. 6078 - 6081 (2013)

A novel method for the synthesis of a wide range of 1,5-disubstituted 1,2-dihydro-1,2,4-triazol-3-ones is described. The key step involves a reaction between a dilithiated BOC-hydrazine and a N-alkoxycarbonylcarboximidothioate. A broad range of aryl and a

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