Cas 853262-03-0,4-N-[2-(N-benzyloxylcarbonylamino)-acetyl]amino-1-(β-D-2,3,5-tri-O-acetylribofuranosyl)imidazole

853262-03-0

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Basic information

Product Name: 4-N-[2-(N-benzyloxylcarbonylamino)-acetyl]amino-1-(β-D-2,3,5-tri-O-acetylribofuranosyl)imidazole
Synonyms:
CAS NO:853262-03-0
Molecular Formula:
Molecular Weight: 532.507
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: 4-N-[2-(N-benzyloxylcarbonylamino)-acetyl]amino-1-(β-D-2,3,5-tri-O-acetylribofuranosyl)imidazole(CAS DataBase Reference)
NIST Chemistry Reference: 4-N-[2-(N-benzyloxylcarbonylamino)-acetyl]amino-1-(β-D-2,3,5-tri-O-acetylribofuranosyl)imidazole(853262-03-0)
EPA Substance Registry System: 4-N-[2-(N-benzyloxylcarbonylamino)-acetyl]amino-1-(β-D-2,3,5-tri-O-acetylribofuranosyl)imidazole(853262-03-0)

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: 853262-03-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 853262-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,3,2,6 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 853262-03:
(8*8)+(7*5)+(6*3)+(5*2)+(4*6)+(3*2)+(2*0)+(1*3)=160
160 % 10 = 0
So 853262-03-0 is a valid CAS Registry Number.

853262-03-0Upstream product

853262-03-0Downstream Products

853262-03-0Relevant academic research and scientific papers

Synthesis of ribavirin analogues containing amino-acid residues

Li, Daliang,Bao, Hongli,Tan, Qitao,Cai, Dongmei,You, Tianpa

, p. 1017 - 1026 (2007/10/03)

A convenient procedure for coupling 1,2,3,5-tetra-O-acetyl-β-D- ribofuranose and 4-nitroimidazole was developed to obtain β-anomer as the major product. A novel category of nucleoside analogues with the introduction of natural L-amino acids to the base mo

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