Cas 156126-53-3,9-((1R,2R,3S)-2,3-bis(hydroxymethyl)cyclobutyl)-2-amino-1H-purin-6(9H)-one

156126-53-3

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Basic information

Product Name: 9-((1R,2R,3S)-2,3-bis(hydroxymethyl)cyclobutyl)-2-amino-1H-purin-6(9H)-one
Synonyms: 9-((1R,2R,3S)-2,3-bis(hydroxymethyl)cyclobutyl)-2-amino-1H-purin-6(9H)-one
CAS NO:156126-53-3
Molecular Formula:
Molecular Weight: 473.488
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: 9-((1R,2R,3S)-2,3-bis(hydroxymethyl)cyclobutyl)-2-amino-1H-purin-6(9H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 9-((1R,2R,3S)-2,3-bis(hydroxymethyl)cyclobutyl)-2-amino-1H-purin-6(9H)-one(156126-53-3)
EPA Substance Registry System: 9-((1R,2R,3S)-2,3-bis(hydroxymethyl)cyclobutyl)-2-amino-1H-purin-6(9H)-one(156126-53-3)

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: 156126-53-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 156126-53-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,1,2 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 156126-53:
(8*1)+(7*5)+(6*6)+(5*1)+(4*2)+(3*6)+(2*5)+(1*3)=123
123 % 10 = 3
So 156126-53-3 is a valid CAS Registry Number.

156126-53-3Upstream product

156126-83-9 <1S-(1α,2β,3α)>-3-(2-Amino-6-iodo-9H-purin-9-yl)-1,2-cyclobutanedimethanol dibenzoate ester

156126-53-3Downstream Products

156126-53-3Relevant academic research and scientific papers

Expedient approach to chiral cyclobutanones: Asymmetric synthesis of cyclobut-G

Darses, Benjamin,Greene, Andrew E.,Coote, Susannah C.,Poisson, Jean-Francois

, p. 821 - 824 (2008)

An efficient one-pot asymmetric synthesis of cyclobutanones from chiral enol ethers is described. The approach is illustrated with alkyl- and functionalized alkyl-substituted enol ethers (nine examples). A new enantioselective synthesis of cyclobut-G (Lobucavir) could thus be achieved.

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