Cas 536741-60-3,(1'R,4'S)-1'-(6-chloro-9H-purin-9-yl)-4'-[nitro(phenylsulfonyl)-[13C]methyl]cyclopent-2'-ene

536741-60-3

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Basic information

Product Name: (1'R,4'S)-1'-(6-chloro-9H-purin-9-yl)-4'-[nitro(phenylsulfonyl)-[13C]methyl]cyclopent-2'-ene
Synonyms: (1'R,4'S)-1'-(6-chloro-9H-purin-9-yl)-4'-[nitro(phenylsulfonyl)-[13C]methyl]cyclopent-2'-ene
CAS NO:536741-60-3
Molecular Formula:
Molecular Weight: 420.837
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: (1'R,4'S)-1'-(6-chloro-9H-purin-9-yl)-4'-[nitro(phenylsulfonyl)-[13C]methyl]cyclopent-2'-ene(CAS DataBase Reference)
NIST Chemistry Reference: (1'R,4'S)-1'-(6-chloro-9H-purin-9-yl)-4'-[nitro(phenylsulfonyl)-[13C]methyl]cyclopent-2'-ene(536741-60-3)
EPA Substance Registry System: (1'R,4'S)-1'-(6-chloro-9H-purin-9-yl)-4'-[nitro(phenylsulfonyl)-[13C]methyl]cyclopent-2'-ene(536741-60-3)

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: 536741-60-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 536741-60-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,6,7,4 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 536741-60:
(8*5)+(7*3)+(6*6)+(5*7)+(4*4)+(3*1)+(2*6)+(1*0)=163
163 % 10 = 3
So 536741-60-3 is a valid CAS Registry Number.

536741-60-3Upstream product

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536741-60-3Relevant academic research and scientific papers

Synthesis of enantiomerically-pure [13C]aristeromycylcobalamin and its reactivity in dioldehydratase, glyceroldehydratase, ethanolamine ammonia-lyase and methylmalonyl-CoA mutase reactions

Weigl, Ulrich,Heimberger, Martin,Pierik, Antonio J.,Retey, Janos

, p. 652 - 660 (2003)

We describe a novel enantio-selective synthesis of aristeromycin, the carbocyclic analogue of adenosine. The seven-step synthesis is also suitable for the preparation of specifically-labelled [6′-13C]aristeromycin. Both the unlabelled and

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