Cas 1208237-17-5,(S)-3-(3-hydroxyphenyl)-2-((S)-3-(1-methoxy-4-methyl-1-oxopentan-2-yl)ureido)propanoic acid

1208237-17-5

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Basic information

Product Name: (S)-3-(3-hydroxyphenyl)-2-((S)-3-(1-methoxy-4-methyl-1-oxopentan-2-yl)ureido)propanoic acid
Synonyms:
CAS NO:1208237-17-5
Molecular Formula:
Molecular Weight: 352.387
EINECS: N/A
Product Categories: N/A
Mol File: 1208237-17-5.mol
Article Data: 1

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: (S)-3-(3-hydroxyphenyl)-2-((S)-3-(1-methoxy-4-methyl-1-oxopentan-2-yl)ureido)propanoic acid(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-(3-hydroxyphenyl)-2-((S)-3-(1-methoxy-4-methyl-1-oxopentan-2-yl)ureido)propanoic acid(1208237-17-5)
EPA Substance Registry System: (S)-3-(3-hydroxyphenyl)-2-((S)-3-(1-methoxy-4-methyl-1-oxopentan-2-yl)ureido)propanoic acid(1208237-17-5)

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: 1208237-17-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1208237-17-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,8,2,3 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1208237-17:
(9*1)+(8*2)+(7*0)+(6*8)+(5*2)+(4*3)+(3*7)+(2*1)+(1*7)=125
125 % 10 = 5
So 1208237-17-5 is a valid CAS Registry Number.

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1208237-17-5Relevant articles and documents

Bioisosterism of urea-based GCPII inhibitors: Synthesis and structure-activity relationship studies

Wang, Haofan,Byun, Youngjoo,Barinka, Cyril,Pullambhatla, Mrudula,Bhang, Hyo-eun C.,Fox, James J.,Lubkowski, Jacek,Mease, Ronnie C.,Pomper, Martin G.

supporting information; experimental part, p. 392 - 397 (2010/04/02)

We report a strategy based on bioisosterism to improve the physicochemical properties of existing hydrophilic, urea-based GCPII inhibitors. Comprehensive structure-activity relationship studies of the P1′ site of ZJ-43- and DCIBzL-based compounds identifi

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