Cas 1027306-94-0,2-[(R)-1-Amino-2-(1H-indol-3-yl)-ethyl]-5-phenyl-1H-imidazole-4-carboxylic acid ethyl ester

1027306-94-0

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Basic information

Product Name: 2-[(R)-1-Amino-2-(1H-indol-3-yl)-ethyl]-5-phenyl-1H-imidazole-4-carboxylic acid ethyl ester
Synonyms: 2-[(R)-1-Amino-2-(1H-indol-3-yl)-ethyl]-5-phenyl-1H-imidazole-4-carboxylic acid ethyl ester
CAS NO:1027306-94-0
Molecular Formula:
Molecular Weight: 374.442
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-[(R)-1-Amino-2-(1H-indol-3-yl)-ethyl]-5-phenyl-1H-imidazole-4-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-[(R)-1-Amino-2-(1H-indol-3-yl)-ethyl]-5-phenyl-1H-imidazole-4-carboxylic acid ethyl ester(1027306-94-0)
EPA Substance Registry System: 2-[(R)-1-Amino-2-(1H-indol-3-yl)-ethyl]-5-phenyl-1H-imidazole-4-carboxylic acid ethyl ester(1027306-94-0)

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: 1027306-94-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1027306-94-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,3,0 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1027306-94:
(9*1)+(8*0)+(7*2)+(6*7)+(5*3)+(4*0)+(3*6)+(2*9)+(1*4)=120
120 % 10 = 0
So 1027306-94-0 is a valid CAS Registry Number.

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1027306-94-0Relevant academic research and scientific papers

Azole endothelin antagonists. 1. A receptor model explains an unusual structure-activity profile

Von Geldern, Thomas W.,Hutchins, Charles,Kester, Jeffrey A.,Wu-Wong, Jinshyun R.,Chiou, William,Dixon, Douglas B.,Opgenorth, Terry J.

, p. 957 - 967 (2007/10/03)

The pseudotetrapeptide FR-139317 is a potent and highly selective antagonist of the endothelin-A (ET(A)) receptor; however, its peptidic nature leads to poor oral absorption characteristics which make it an unlikely drug candidate. In an attempt to improv

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