Cas 179929-16-9,2-(Acetyl-tert-butoxycarbonyl-amino)-6-[(2R,3R,4R,5R)-3,4-diacetoxy-5-(6-benzoylamino-purin-9-yl)-tetrahydro-furan-2-yl]-hexanoic acid methyl ester

179929-16-9

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Basic information

Product Name: 2-(Acetyl-tert-butoxycarbonyl-amino)-6-[(2R,3R,4R,5R)-3,4-diacetoxy-5-(6-benzoylamino-purin-9-yl)-tetrahydro-furan-2-yl]-hexanoic acid methyl ester
Synonyms: 2-(Acetyl-tert-butoxycarbonyl-amino)-6-[(2R,3R,4R,5R)-3,4-diacetoxy-5-(6-benzoylamino-purin-9-yl)-tetrahydro-furan-2-yl]-hexanoic acid methyl ester
CAS NO:179929-16-9
Molecular Formula:
Molecular Weight: 710.741
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: 2-(Acetyl-tert-butoxycarbonyl-amino)-6-[(2R,3R,4R,5R)-3,4-diacetoxy-5-(6-benzoylamino-purin-9-yl)-tetrahydro-furan-2-yl]-hexanoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-(Acetyl-tert-butoxycarbonyl-amino)-6-[(2R,3R,4R,5R)-3,4-diacetoxy-5-(6-benzoylamino-purin-9-yl)-tetrahydro-furan-2-yl]-hexanoic acid methyl ester(179929-16-9)
EPA Substance Registry System: 2-(Acetyl-tert-butoxycarbonyl-amino)-6-[(2R,3R,4R,5R)-3,4-diacetoxy-5-(6-benzoylamino-purin-9-yl)-tetrahydro-furan-2-yl]-hexanoic acid methyl ester(179929-16-9)

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: 179929-16-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 179929-16-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,9,2 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 179929-16:
(8*1)+(7*7)+(6*9)+(5*9)+(4*2)+(3*9)+(2*1)+(1*6)=199
199 % 10 = 9
So 179929-16-9 is a valid CAS Registry Number.

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179929-16-9Relevant academic research and scientific papers

Relationship between chemical structure and antileishmanial effect of sinefungine analogues

Blanchard,El Kortbi,Fourrey,Lawrence,Robert-Gero

, p. 1121 - 1135 (2007/10/03)

The synthesis of various analogues of sinefungin (1), having structures 2- 5, has been developed by means of an original approach which uses radical chemistry. The study of their biological activities revealed that for the antileishmanial effect of sinefungin, the presence of the amino group at C- 6' in the (S)-configuration and the presence of the carboxyl group at C-9' are necessary.

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