Cas 1025829-54-2,2-[(R)-1-Benzyloxycarbonylamino-2-(1H-indol-3-yl)-ethyl]-5-propyl-oxazole-4-carboxylic acid ethyl ester

1025829-54-2

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Basic information

Product Name: 2-[(R)-1-Benzyloxycarbonylamino-2-(1H-indol-3-yl)-ethyl]-5-propyl-oxazole-4-carboxylic acid ethyl ester
Synonyms:
CAS NO:1025829-54-2
Molecular Formula:
Molecular Weight: 475.544
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-Benzyloxycarbonylamino-2-(1H-indol-3-yl)-ethyl]-5-propyl-oxazole-4-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-[(R)-1-Benzyloxycarbonylamino-2-(1H-indol-3-yl)-ethyl]-5-propyl-oxazole-4-carboxylic acid ethyl ester(1025829-54-2)
EPA Substance Registry System: 2-[(R)-1-Benzyloxycarbonylamino-2-(1H-indol-3-yl)-ethyl]-5-propyl-oxazole-4-carboxylic acid ethyl ester(1025829-54-2)

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: 1025829-54-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1025829-54-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,5,8,2 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1025829-54:
(9*1)+(8*0)+(7*2)+(6*5)+(5*8)+(4*2)+(3*9)+(2*5)+(1*4)=142
142 % 10 = 2
So 1025829-54-2 is a valid CAS Registry Number.

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1025829-54-2Relevant 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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