Cas 652173-18-7,9-benzyl-6-(4'-azido-4'-deoxy-β-L-rhamnopyranosylamino)-9H-purine

652173-18-7

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Basic information

Product Name: 9-benzyl-6-(4'-azido-4'-deoxy-β-L-rhamnopyranosylamino)-9H-purine
Synonyms: 9-benzyl-6-(4'-azido-4'-deoxy-β-L-rhamnopyranosylamino)-9H-purine
CAS NO:652173-18-7
Molecular Formula:
Molecular Weight: 396.409
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: 9-benzyl-6-(4'-azido-4'-deoxy-β-L-rhamnopyranosylamino)-9H-purine(CAS DataBase Reference)
NIST Chemistry Reference: 9-benzyl-6-(4'-azido-4'-deoxy-β-L-rhamnopyranosylamino)-9H-purine(652173-18-7)
EPA Substance Registry System: 9-benzyl-6-(4'-azido-4'-deoxy-β-L-rhamnopyranosylamino)-9H-purine(652173-18-7)

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: 652173-18-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 652173-18-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,2,1,7 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 652173-18:
(8*6)+(7*5)+(6*2)+(5*1)+(4*7)+(3*3)+(2*1)+(1*8)=147
147 % 10 = 7
So 652173-18-7 is a valid CAS Registry Number.

652173-18-7Upstream product

4261-14-7 9-benzyl-9H-purin-6-ylamine

652173-18-7Downstream Products

1053693-91-6 (2S,3R,4R,5R,6S)-5-Amino-2-(9-benzyl-9H-purin-6-ylamino)-6-methyl-tetrahydro-pyran-3,4-diol

652173-18-7Relevant academic research and scientific papers

An approach to the generation of simple analogues of the antitumour agent spicamycin.

Mons, Stephane,Fleet, George W J

, p. 3685 - 3691 (2003)

The one-step glycosylation of arylamines in acidic medium is extended to adenine derivatives for the first time, providing a considerable improvement over existing reactions. This method is used to prepare some rhamnospicamycin analogues containing differ

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