Cas 117175-52-7,4-amino-7-(β-D-ribofuranosyl)pyrrolo<2,3-d>pyrimidine-5-carboxy-L-phenylalanine amide

117175-52-7

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Basic information

Product Name: 4-amino-7-(β-D-ribofuranosyl)pyrrolo<2,3-d>pyrimidine-5-carboxy-L-phenylalanine amide
Synonyms: 4-amino-7-(β-D-ribofuranosyl)pyrrolo<2,3-d>pyrimidine-5-carboxy-L-phenylalanine amide
CAS NO:117175-52-7
Molecular Formula:
Molecular Weight: 456.458
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-amino-7-(β-D-ribofuranosyl)pyrrolo<2,3-d>pyrimidine-5-carboxy-L-phenylalanine amide(CAS DataBase Reference)
NIST Chemistry Reference: 4-amino-7-(β-D-ribofuranosyl)pyrrolo<2,3-d>pyrimidine-5-carboxy-L-phenylalanine amide(117175-52-7)
EPA Substance Registry System: 4-amino-7-(β-D-ribofuranosyl)pyrrolo<2,3-d>pyrimidine-5-carboxy-L-phenylalanine amide(117175-52-7)

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: 117175-52-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 117175-52-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,1,7 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 117175-52:
(8*1)+(7*1)+(6*7)+(5*1)+(4*7)+(3*5)+(2*5)+(1*2)=117
117 % 10 = 7
So 117175-52-7 is a valid CAS Registry Number.

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117175-52-7Relevant academic research and scientific papers

NUCLEOSIDE PEPTIDES - IX. SYNTHESIS OF PEPTIDE DERIVATIVES OF SANGIVAMYCIC ACID AND DEAMINOSANGIVAMYCIC ACID

Ramasamy, Kandasamy,Robins, Roland K.,Revankar, Ganapathi R.

, p. 1023 - 1034 (2007/10/02)

A number of amino acid and peptide conjugates of sangivamycic acid (4) and deaminosangivamycic (6) have been prepared in which the peptide linkage is on the carboxylic group of the aglycon moiety.The synthesis of these nucleoside peptides was accomplished

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