Cas 874947-19-0,1-Piperidinecarboxylic acid, 4-[2-[2-(bromoacetyl)hydrazino]-2-oxo-1-phenylethylidene]-, 1,1-dimethylethyl ester

874947-19-0

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Basic information

Product Name: 1-Piperidinecarboxylic acid, 4-[2-[2-(bromoacetyl)hydrazino]-2-oxo-1-phenylethylidene]-, 1,1-dimethylethyl ester
Synonyms:
CAS NO:874947-19-0
Molecular Formula: C20H26BrN3O4
Molecular Weight: 452.348
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-Piperidinecarboxylic acid, 4-[2-[2-(bromoacetyl)hydrazino]-2-oxo-1-phenylethylidene]-, 1,1-dimethylethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1-Piperidinecarboxylic acid, 4-[2-[2-(bromoacetyl)hydrazino]-2-oxo-1-phenylethylidene]-, 1,1-dimethylethyl ester(874947-19-0)
EPA Substance Registry System: 1-Piperidinecarboxylic acid, 4-[2-[2-(bromoacetyl)hydrazino]-2-oxo-1-phenylethylidene]-, 1,1-dimethylethyl ester(874947-19-0)

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: 874947-19-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 874947-19-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,9,4 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 874947-19:
(8*8)+(7*7)+(6*4)+(5*9)+(4*4)+(3*7)+(2*1)+(1*9)=230
230 % 10 = 0
So 874947-19-0 is a valid CAS Registry Number.

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874947-19-0Relevant academic research and scientific papers

General synthesis of tetrasubstituted alkenyl-1,3,4-oxadiazoles

James, Clint A.,Poirier, Brigitte,Grisé, Christiane,Martel, Alain,Ruediger, Edward H.

, p. 511 - 514 (2007/10/03)

Tetrasubstituted alkenyl-1,3,4-oxadiazoles were synthesized in moderate to excellent yield, under mild conditions and in the presence of sensitive functional groups, via the cyclization of diacylhydrazides using PPh3 and hexachloroethane in the

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