Cas 225641-89-4,[(1R,3R)-3-(4-Cyano-4-phenyl-piperidin-1-yl)-cyclopentyl]-carbamic acid tert-butyl ester

225641-89-4

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Basic information

Product Name: [(1R,3R)-3-(4-Cyano-4-phenyl-piperidin-1-yl)-cyclopentyl]-carbamic acid tert-butyl ester
Synonyms:
CAS NO:225641-89-4
Molecular Formula:
Molecular Weight: 369.507
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: [(1R,3R)-3-(4-Cyano-4-phenyl-piperidin-1-yl)-cyclopentyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(1R,3R)-3-(4-Cyano-4-phenyl-piperidin-1-yl)-cyclopentyl]-carbamic acid tert-butyl ester(225641-89-4)
EPA Substance Registry System: [(1R,3R)-3-(4-Cyano-4-phenyl-piperidin-1-yl)-cyclopentyl]-carbamic acid tert-butyl ester(225641-89-4)

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: 225641-89-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 225641-89-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,5,6,4 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 225641-89:
(8*2)+(7*2)+(6*5)+(5*6)+(4*4)+(3*1)+(2*8)+(1*9)=134
134 % 10 = 4
So 225641-89-4 is a valid CAS Registry Number.

225641-89-4Upstream product

225641-84-9 tert-butyl N-[(1R,3S)-3-hydroxycyclopentyl]carbamate

225641-89-4Downstream Products

225641-89-4Relevant academic research and scientific papers

Preparation and evaluation of 1,3-diaminocyclopentane-linked dihydropyrimidinone derivatives as selective α(1a)-receptor

Barrow, James C.,Glass, Kristen L.,Selnick, Harold G.,Freidinger, Roger M.,Chang, Raymond S.L.,O'Malley, Stacey S.,Woyden, Carla

, p. 1917 - 1920 (2000)

Several 1,3-diaminocyclopentane linked α(1a)-receptor antagonists were prepared using a divergent chemical strategy that allows for rapid analysis of all stereochemical permutations for their effect on α1-receptor binding. (C) 2000 Published by Elsevier Science Ltd.

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