Cas 173033-98-2,Benzoic acid (2R,3S,5R)-5-(2-isobutyrylamino-6-oxo-1,6-dihydro-purin-9-yl)-2-methylsulfanylmethoxymethyl-tetrahydro-furan-3-yl ester

173033-98-2

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Basic information

Product Name: Benzoic acid (2R,3S,5R)-5-(2-isobutyrylamino-6-oxo-1,6-dihydro-purin-9-yl)-2-methylsulfanylmethoxymethyl-tetrahydro-furan-3-yl ester
Synonyms: Benzoic acid (2R,3S,5R)-5-(2-isobutyrylamino-6-oxo-1,6-dihydro-purin-9-yl)-2-methylsulfanylmethoxymethyl-tetrahydro-furan-3-yl ester
CAS NO:173033-98-2
Molecular Formula:
Molecular Weight: 501.563
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: Benzoic acid (2R,3S,5R)-5-(2-isobutyrylamino-6-oxo-1,6-dihydro-purin-9-yl)-2-methylsulfanylmethoxymethyl-tetrahydro-furan-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid (2R,3S,5R)-5-(2-isobutyrylamino-6-oxo-1,6-dihydro-purin-9-yl)-2-methylsulfanylmethoxymethyl-tetrahydro-furan-3-yl ester(173033-98-2)
EPA Substance Registry System: Benzoic acid (2R,3S,5R)-5-(2-isobutyrylamino-6-oxo-1,6-dihydro-purin-9-yl)-2-methylsulfanylmethoxymethyl-tetrahydro-furan-3-yl ester(173033-98-2)

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: 173033-98-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 173033-98-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,0,3 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 173033-98:
(8*1)+(7*7)+(6*3)+(5*0)+(4*3)+(3*3)+(2*9)+(1*8)=122
122 % 10 = 2
So 173033-98-2 is a valid CAS Registry Number.

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173033-98-2Relevant academic research and scientific papers

A mild method for the syntheses of 3′-thioformacetal dinucleotides: The development of diphenylphosphinate as a glycosyl donor

Zhang, Jiancun,Matteucci, Mark D.

, p. 8375 - 8378 (1995)

A mild and efficient procedure for the syntheses of 3′-thioformacetal dinucleotides is presented. The glycosylation synthon agent, diphenylphosphinate formacetal was developed as the intermediate for the coupling reaction under mild basic conditions. This

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