Cas 1071906-30-3,9-((1S,4R)-4-((bis(4-Methoxyphenyl)(phenyl)Methoxy)Methyl)cyclopent-2-enyl)-5,9-dihydro-4H-purin-6-aMine

1071906-30-3

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Basic information

Product Name: 9-((1S,4R)-4-((bis(4-Methoxyphenyl)(phenyl)Methoxy)Methyl)cyclopent-2-enyl)-5,9-dihydro-4H-purin-6-aMine
Synonyms: 9-((1S,4R)-4-((bis(4-Methoxyphenyl)(phenyl)Methoxy)Methyl)cyclopent-2-enyl)-5,9-dihydro-4H-purin-6-aMine
CAS NO:1071906-30-3
Molecular Formula:
Molecular Weight: 535.63612
EINECS: N/A
Product Categories: N/A
Mol File: 1071906-30-3.mol

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: 9-((1S,4R)-4-((bis(4-Methoxyphenyl)(phenyl)Methoxy)Methyl)cyclopent-2-enyl)-5,9-dihydro-4H-purin-6-aMine(CAS DataBase Reference)
NIST Chemistry Reference: 9-((1S,4R)-4-((bis(4-Methoxyphenyl)(phenyl)Methoxy)Methyl)cyclopent-2-enyl)-5,9-dihydro-4H-purin-6-aMine(1071906-30-3)
EPA Substance Registry System: 9-((1S,4R)-4-((bis(4-Methoxyphenyl)(phenyl)Methoxy)Methyl)cyclopent-2-enyl)-5,9-dihydro-4H-purin-6-aMine(1071906-30-3)

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: 1071906-30-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1071906-30-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,1,9,0 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1071906-30:
(9*1)+(8*0)+(7*7)+(6*1)+(5*9)+(4*0)+(3*6)+(2*3)+(1*0)=133
133 % 10 = 3
So 1071906-30-3 is a valid CAS Registry Number.

1071906-30-3Upstream product

1071906-30-3Downstream Products

220285-03-0 [(1R,3S)-3-(6-amino-9H-purin-9-yl)cyclopentyl]methanol

1071906-30-3Relevant academic research and scientific papers

Synthesis of D- And L-carbocyclic nucleosides via rhodium-catalyzed asymmetric hydroacylation as the key step

Marce, Patricia,Diaz, Yolanda,Matheu, M. Isabel,Castillon, Sergio

supporting information; experimental part, p. 4735 - 4738 (2009/05/31)

(Chemical Equation Presented) D- and L-carbocyclic nucleosides were obtained by a new procedure involving an enantioselective rhodium/duphos- catalyzed hydroacylation reaction as the key step. The 3-hydroxymethyl- cyclopentanol intermediate was obtained by stereoselective reduction of ketone and by dynamic kinetic resolution (DKR).

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