Cas 888015-87-0,(1S,2S,3S,5S)-5-(2-amino-6-chloropyrimidin-4-yl)amino-3-(benzyloxy)-2-(benzyloxymethyl)cyclopentanol

888015-87-0

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Basic information

Product Name: (1S,2S,3S,5S)-5-(2-amino-6-chloropyrimidin-4-yl)amino-3-(benzyloxy)-2-(benzyloxymethyl)cyclopentanol
Synonyms: (1S,2S,3S,5S)-5-(2-amino-6-chloropyrimidin-4-yl)amino-3-(benzyloxy)-2-(benzyloxymethyl)cyclopentanol
CAS NO:888015-87-0
Molecular Formula:
Molecular Weight: 454.956
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: (1S,2S,3S,5S)-5-(2-amino-6-chloropyrimidin-4-yl)amino-3-(benzyloxy)-2-(benzyloxymethyl)cyclopentanol(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2S,3S,5S)-5-(2-amino-6-chloropyrimidin-4-yl)amino-3-(benzyloxy)-2-(benzyloxymethyl)cyclopentanol(888015-87-0)
EPA Substance Registry System: (1S,2S,3S,5S)-5-(2-amino-6-chloropyrimidin-4-yl)amino-3-(benzyloxy)-2-(benzyloxymethyl)cyclopentanol(888015-87-0)

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: 888015-87-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 888015-87-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,8,0,1 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 888015-87:
(8*8)+(7*8)+(6*8)+(5*0)+(4*1)+(3*5)+(2*8)+(1*7)=210
210 % 10 = 0
So 888015-87-0 is a valid CAS Registry Number.

888015-87-0Upstream product

888015-87-0Downstream Products

888015-90-5 2-amino-4-methoxy-6-[(1α,2β,3α,4β)-2-hydroxy-4-(phenylmethoxy)-3-[(phenylmethoxy)methyl]cyclopentyl]amino-5-aminopyrimidine

888015-87-0Relevant academic research and scientific papers

Synthesis of [14C]-radiolabelled entecavir

Ogan, Marc D.,Kucera, David J.,Pendri, Yadagiri R.,Rinehart, J. Kent

, p. 645 - 655 (2005)

Radiolabelled [l4C]entecavir, (1), was prepared in 12 steps from (1S,2R,3S,5R)-3-(benzyloxy)-2-(benzyloxymethyl)-6-oxa-bicyclo[3.1.0]hexane 2. The chemical yield of [l4C]entecavir was 14% from the epoxide 2. Introduction of [14

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