Cas 252297-65-7,{5-<i>tert</i>-butoxycarbonylamino-5-[1-(2-oxo-2-phenyl-ethyl)-4-phenyl-1<i>H</i>-imidazol-2-yl]-pentyl}-carbamic acid benzyl ester

252297-65-7

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Basic information

Product Name: {5-tert-butoxycarbonylamino-5-[1-(2-oxo-2-phenyl-ethyl)-4-phenyl-1H-imidazol-2-yl]-pentyl}-carbamic acid benzyl ester
Synonyms:
CAS NO:252297-65-7
Molecular Formula:
Molecular Weight: 596.726
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: {5-tert-butoxycarbonylamino-5-[1-(2-oxo-2-phenyl-ethyl)-4-phenyl-1H-imidazol-2-yl]-pentyl}-carbamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {5-tert-butoxycarbonylamino-5-[1-(2-oxo-2-phenyl-ethyl)-4-phenyl-1H-imidazol-2-yl]-pentyl}-carbamic acid benzyl ester(252297-65-7)
EPA Substance Registry System: {5-tert-butoxycarbonylamino-5-[1-(2-oxo-2-phenyl-ethyl)-4-phenyl-1H-imidazol-2-yl]-pentyl}-carbamic acid benzyl ester(252297-65-7)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 252297-65-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 252297-65-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,2,2,9 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 252297-65:
(8*2)+(7*5)+(6*2)+(5*2)+(4*9)+(3*7)+(2*6)+(1*5)=147
147 % 10 = 7
So 252297-65-7 is a valid CAS Registry Number.

252297-65-7Upstream product

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252297-65-7Relevant academic research and scientific papers

Synthesis of substituted imidazopyrazines as ligands for the human somatostatin receptor subtype 5

Contour-Galcera, Marie-Odile,Poitout, Lydie,Moinet, Christophe,Morgan, Barry,Gordon, Tom,Roubert, Pierre,Thurieau, Christophe

, p. 741 - 745 (2001)

A new preparation of trisubstituted imidazopyrazines and dihydroimidazopyrazines via parallel synthesis using aminoacids and bromoketones resulted in the discovery of non-peptidic sst5 selective agonists.

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