Cas 141956-73-2,2-(3-{3-[1-(2-Cyano-ethyl)-3-(1-methoxycarbonyl-2-phenyl-ethyl)-ureido]-propyl}-3-phenyl-ureido)-3-phenyl-propionic acid methyl ester

141956-73-2

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Basic information

Product Name: 2-(3-{3-[1-(2-Cyano-ethyl)-3-(1-methoxycarbonyl-2-phenyl-ethyl)-ureido]-propyl}-3-phenyl-ureido)-3-phenyl-propionic acid methyl ester
Synonyms:
CAS NO:141956-73-2
Molecular Formula:
Molecular Weight: 613.714
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: 2-(3-{3-[1-(2-Cyano-ethyl)-3-(1-methoxycarbonyl-2-phenyl-ethyl)-ureido]-propyl}-3-phenyl-ureido)-3-phenyl-propionic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-(3-{3-[1-(2-Cyano-ethyl)-3-(1-methoxycarbonyl-2-phenyl-ethyl)-ureido]-propyl}-3-phenyl-ureido)-3-phenyl-propionic acid methyl ester(141956-73-2)
EPA Substance Registry System: 2-(3-{3-[1-(2-Cyano-ethyl)-3-(1-methoxycarbonyl-2-phenyl-ethyl)-ureido]-propyl}-3-phenyl-ureido)-3-phenyl-propionic acid methyl ester(141956-73-2)

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: 141956-73-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 141956-73-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,9,5 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 141956-73:
(8*1)+(7*4)+(6*1)+(5*9)+(4*5)+(3*6)+(2*7)+(1*3)=142
142 % 10 = 2
So 141956-73-2 is a valid CAS Registry Number.

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141956-73-2Relevant academic research and scientific papers

Molecular Scaffolds I: Intramolecular Hydrogen Bonding in a Family of Di- and Triureas

Nowick, James S.,Powell, Noel A.,Martinez, Eduardo J.,Smith, Eric M.,Noronha, Glenn

, p. 3763 - 3765 (2007/10/02)

Di- and triurea derivatives 1 can be prepared by an iterative procedure and are found to exist in intramolecularly hydrogen bonded 10-membered ring conformations, in which substituents R1 and R2 and hydrogen bonding control the direction of the urea carbonyl groups.

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