Cas 201848-20-6,N-[6-Hydroxy-9-((1R,3S,4R)-3-hydroxy-4-trityloxymethyl-cyclopentyl)-9H-purin-2-yl]-isobutyramide

201848-20-6

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Basic information

Product Name: N-[6-Hydroxy-9-((1R,3S,4R)-3-hydroxy-4-trityloxymethyl-cyclopentyl)-9H-purin-2-yl]-isobutyramide
Synonyms: N-[6-Hydroxy-9-((1R,3S,4R)-3-hydroxy-4-trityloxymethyl-cyclopentyl)-9H-purin-2-yl]-isobutyramide
CAS NO:201848-20-6
Molecular Formula:
Molecular Weight: 577.683
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: N-[6-Hydroxy-9-((1R,3S,4R)-3-hydroxy-4-trityloxymethyl-cyclopentyl)-9H-purin-2-yl]-isobutyramide(CAS DataBase Reference)
NIST Chemistry Reference: N-[6-Hydroxy-9-((1R,3S,4R)-3-hydroxy-4-trityloxymethyl-cyclopentyl)-9H-purin-2-yl]-isobutyramide(201848-20-6)
EPA Substance Registry System: N-[6-Hydroxy-9-((1R,3S,4R)-3-hydroxy-4-trityloxymethyl-cyclopentyl)-9H-purin-2-yl]-isobutyramide(201848-20-6)

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: 201848-20-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 201848-20-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,8,4 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 201848-20:
(8*2)+(7*0)+(6*1)+(5*8)+(4*4)+(3*8)+(2*2)+(1*0)=106
106 % 10 = 6
So 201848-20-6 is a valid CAS Registry Number.

201848-20-6Upstream product

201848-20-6Downstream Products

201848-25-1 Acetic acid (1S,2R,4R)-4-(6-hydroxy-2-isobutyrylamino-purin-9-yl)-2-trityloxymethyl-cyclopentyl ester

201848-20-6Relevant academic research and scientific papers

Synthesis of the optically active carbocyclic analogs of the four 2'- deoxyribonucleoslde monophosphates

Schmitt, Laurent,Caperelli, Carol A.

, p. 2165 - 2192 (1997)

The (+)-enantiomer of the carbocyclic analogs of the four 2'-deoxy- ribonucleoside monophosphate constituents of DNA, C-dAMP2 (1: A), C-dGMP (1: G), C-dCMP (1: C), and C-TMP (1: T) have been synthesized via the Mitsunobu coupling reaction. Two

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