Cas 943763-22-2,ethyl 2-{[benzyl(cyano)amino]methyl}-3-(2-chlorophenyl)-3-hydroxypropionate

943763-22-2

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Basic information

Product Name: ethyl 2-{[benzyl(cyano)amino]methyl}-3-(2-chlorophenyl)-3-hydroxypropionate
Synonyms: ethyl 2-{[benzyl(cyano)amino]methyl}-3-(2-chlorophenyl)-3-hydroxypropionate
CAS NO:943763-22-2
Molecular Formula:
Molecular Weight: 372.851
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: ethyl 2-{[benzyl(cyano)amino]methyl}-3-(2-chlorophenyl)-3-hydroxypropionate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 2-{[benzyl(cyano)amino]methyl}-3-(2-chlorophenyl)-3-hydroxypropionate(943763-22-2)
EPA Substance Registry System: ethyl 2-{[benzyl(cyano)amino]methyl}-3-(2-chlorophenyl)-3-hydroxypropionate(943763-22-2)

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: 943763-22-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 943763-22-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,7,6 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 943763-22:
(8*9)+(7*4)+(6*3)+(5*7)+(4*6)+(3*3)+(2*2)+(1*2)=192
192 % 10 = 2
So 943763-22-2 is a valid CAS Registry Number.

943763-22-2Upstream product

943763-22-2Downstream Products

943763-22-2Relevant academic research and scientific papers

Sodium hydride mediated cascade reaction towards the synthesis of 1,5-disubstituted uracil from cyanamides derived from Baylis-Hillman adducts

Nag,Yadav,Maulik,Batra

, p. 911 - 917 (2007/12/27)

The substituted cyanamides generated from Baylis-Hillman adducts afford 1,5-disubstituted uracils via a sodium hydride induced cascade reaction involving sequential intramolecular attack of the hydroxy group on the nitrile group, cyclization of the result

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