Cas 214153-66-9,(S)-1-((R)-3,3-Diphenyl-2-phenylmethanesulfonylamino-propionyl)-pyrrolidine-2-carboxylic acid [3-(1-trityl-1H-imidazol-4-yl)-prop-2-ynyl]-amide

214153-66-9

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Basic information

Product Name: (S)-1-((R)-3,3-Diphenyl-2-phenylmethanesulfonylamino-propionyl)-pyrrolidine-2-carboxylic acid [3-(1-trityl-1H-imidazol-4-yl)-prop-2-ynyl]-amide
Synonyms:
CAS NO:214153-66-9
Molecular Formula:
Molecular Weight: 838.042
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: (S)-1-((R)-3,3-Diphenyl-2-phenylmethanesulfonylamino-propionyl)-pyrrolidine-2-carboxylic acid [3-(1-trityl-1H-imidazol-4-yl)-prop-2-ynyl]-amide(CAS DataBase Reference)
NIST Chemistry Reference: (S)-1-((R)-3,3-Diphenyl-2-phenylmethanesulfonylamino-propionyl)-pyrrolidine-2-carboxylic acid [3-(1-trityl-1H-imidazol-4-yl)-prop-2-ynyl]-amide(214153-66-9)
EPA Substance Registry System: (S)-1-((R)-3,3-Diphenyl-2-phenylmethanesulfonylamino-propionyl)-pyrrolidine-2-carboxylic acid [3-(1-trityl-1H-imidazol-4-yl)-prop-2-ynyl]-amide(214153-66-9)

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: 214153-66-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 214153-66-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,1,5 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 214153-66:
(8*2)+(7*1)+(6*4)+(5*1)+(4*5)+(3*3)+(2*6)+(1*6)=99
99 % 10 = 9
So 214153-66-9 is a valid CAS Registry Number.

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214153-66-9Relevant academic research and scientific papers

Noncovalent thrombin inhibitors incorporating an imidazolylethynyl p1

Lee, Koo,Jung, Won-Hyuk,Kang, Myunggyun,Lee, Sung-Hack

, p. 2775 - 2778 (2000)

A series of noncovalent tripeptidic thrombin inhibitors incorporating a unidazolylethynyl moiety at P1 was investigated. A number of compounds of this series were highly potent and selective versus trypsin, and several compounds demonstrated good oral absorption in rats (F=58% for compound 19). (C) 2000 Elsevier Science Ltd.

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