Cas 107670-22-4,2-Pentenoic acid, 2-cyano-3-methyl-5-[(4-methylphenyl)amino]-5-oxo-, ethyl ester

107670-22-4

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Basic information

Product Name: 2-Pentenoic acid, 2-cyano-3-methyl-5-[(4-methylphenyl)amino]-5-oxo-, ethyl ester
Synonyms:
CAS NO:107670-22-4
Molecular Formula: C16H18N2O3
Molecular Weight: 286.331
EINECS: N/A
Product Categories: N/A
Mol File: 107670-22-4.mol

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: 2-Pentenoic acid, 2-cyano-3-methyl-5-[(4-methylphenyl)amino]-5-oxo-, ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-Pentenoic acid, 2-cyano-3-methyl-5-[(4-methylphenyl)amino]-5-oxo-, ethyl ester(107670-22-4)
EPA Substance Registry System: 2-Pentenoic acid, 2-cyano-3-methyl-5-[(4-methylphenyl)amino]-5-oxo-, ethyl ester(107670-22-4)

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: 107670-22-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 107670-22-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,6,7 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 107670-22:
(8*1)+(7*0)+(6*7)+(5*6)+(4*7)+(3*0)+(2*2)+(1*2)=114
114 % 10 = 4
So 107670-22-4 is a valid CAS Registry Number.

107670-22-4Upstream product

107670-22-4Downstream Products

107670-22-4Relevant academic research and scientific papers

THE CHEMISTRY AND SYNTHETIC POTENTIALITIES OF β-KETOANILIDES : REACTIN OF ETHYL CYANOACETATE WITH β-KETOANILIDES

Habashi, Adiba,Ibraheim, Nadia Sobhy,Sherif, Sherif Mourad,Shams, Hoda Zaki,Mohareb, Rafatd Milad

, p. 2463 - 2466 (2007/10/02)

Ethyl cyanoacetate reacts with β-ketoanilides 2a-g to give the simple Knoevenagel condensation products 3a-g.The reactivity of 3a towards a variety of chemical reagents was studied to give, in most cases, polyfuncionally substituted pyridine derivatives.

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