Cas 153565-49-2,Diphenyl-carbamic acid 2-acetylamino-9-((2S,4S)-2-benzyloxymethyl-[1,3]dioxolan-4-yl)-9H-purin-6-yl ester

153565-49-2

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Basic information

Product Name: Diphenyl-carbamic acid 2-acetylamino-9-((2S,4S)-2-benzyloxymethyl-[1,3]dioxolan-4-yl)-9H-purin-6-yl ester
Synonyms: Diphenyl-carbamic acid 2-acetylamino-9-((2S,4S)-2-benzyloxymethyl-[1,3]dioxolan-4-yl)-9H-purin-6-yl ester
CAS NO:153565-49-2
Molecular Formula:
Molecular Weight: 580.6
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: Diphenyl-carbamic acid 2-acetylamino-9-((2S,4S)-2-benzyloxymethyl-[1,3]dioxolan-4-yl)-9H-purin-6-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Diphenyl-carbamic acid 2-acetylamino-9-((2S,4S)-2-benzyloxymethyl-[1,3]dioxolan-4-yl)-9H-purin-6-yl ester(153565-49-2)
EPA Substance Registry System: Diphenyl-carbamic acid 2-acetylamino-9-((2S,4S)-2-benzyloxymethyl-[1,3]dioxolan-4-yl)-9H-purin-6-yl ester(153565-49-2)

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: 153565-49-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 153565-49-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,5,6 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 153565-49:
(8*1)+(7*5)+(6*3)+(5*5)+(4*6)+(3*5)+(2*4)+(1*9)=142
142 % 10 = 2
So 153565-49-2 is a valid CAS Registry Number.

153565-49-2Upstream product

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153565-49-2Relevant academic research and scientific papers

Divergent Asymmetric Syntheses of Dioxolane Nucleoside Analogues

Evans, Colleen A.,Dixit, Dilip M.,Siddiqui, M. Arshad,Jin, Haolun,Tse, H. L. Allan,et al.

, p. 2319 - 2322 (1993)

Oxidative degradation of benzyloxymethylacetals derived from D-mannitol or L-ascorbic acid provides dioxolane intermediate 6 and 7 useful in the synthesis of all the stereoisomers of dioxolane nucleoside analogues.

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