Cas 70515-30-9,(S)-2-Amino-N-[(2S,5R)-5-(6-amino-purin-9-yl)-2,5-dihydro-furan-2-ylmethyl]-3-(4-methoxy-phenyl)-propionamide

70515-30-9

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Basic information

Product Name: (S)-2-Amino-N-[(2S,5R)-5-(6-amino-purin-9-yl)-2,5-dihydro-furan-2-ylmethyl]-3-(4-methoxy-phenyl)-propionamide
Synonyms: (S)-2-Amino-N-[(2S,5R)-5-(6-amino-purin-9-yl)-2,5-dihydro-furan-2-ylmethyl]-3-(4-methoxy-phenyl)-propionamide
CAS NO:70515-30-9
Molecular Formula:
Molecular Weight: 409.448
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: (S)-2-Amino-N-[(2S,5R)-5-(6-amino-purin-9-yl)-2,5-dihydro-furan-2-ylmethyl]-3-(4-methoxy-phenyl)-propionamide(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-Amino-N-[(2S,5R)-5-(6-amino-purin-9-yl)-2,5-dihydro-furan-2-ylmethyl]-3-(4-methoxy-phenyl)-propionamide(70515-30-9)
EPA Substance Registry System: (S)-2-Amino-N-[(2S,5R)-5-(6-amino-purin-9-yl)-2,5-dihydro-furan-2-ylmethyl]-3-(4-methoxy-phenyl)-propionamide(70515-30-9)

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: 70515-30-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 70515-30-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,5,1 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70515-30:
(7*7)+(6*0)+(5*5)+(4*1)+(3*5)+(2*3)+(1*0)=99
99 % 10 = 9
So 70515-30-9 is a valid CAS Registry Number.

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70515-30-9Relevant academic research and scientific papers

SYNTHESIS AND ANTITUMOR ACTIVITY OF CYTOSINE AND ADENINE NUCLEOSIDES OF UNSATURATED 5-(AMINOACYL)AMINOPENTOFURANOSES

Adachi, Takeshi,Arai, Yoshihisa,Inoue, Ichizo,Saneyoshi, Mineo

, p. 67 - 78 (2007/10/02)

Direct synthesis of the 1- and 9-(5-azido-2,3,5-trideoxy-β-D-glycero-pent-2-enofuranosyl) derivatives (3a and 3b) of cytosine and adenine, respectively, has been accomplished via treatment of the corresponding 2',3'-unsaturated nucleosides (1a and 1b) wit

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