Cas 309253-79-0,Acetic acid (2R,3R,4R,5R)-4-acetoxy-5-acetoxymethyl-2-(6-phenylmethanesulfonyl-purin-9-yl)-tetrahydro-furan-3-yl ester

309253-79-0

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Basic information

Product Name: Acetic acid (2R,3R,4R,5R)-4-acetoxy-5-acetoxymethyl-2-(6-phenylmethanesulfonyl-purin-9-yl)-tetrahydro-furan-3-yl ester
Synonyms:
CAS NO:309253-79-0
Molecular Formula:
Molecular Weight: 532.531
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: Acetic acid (2R,3R,4R,5R)-4-acetoxy-5-acetoxymethyl-2-(6-phenylmethanesulfonyl-purin-9-yl)-tetrahydro-furan-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (2R,3R,4R,5R)-4-acetoxy-5-acetoxymethyl-2-(6-phenylmethanesulfonyl-purin-9-yl)-tetrahydro-furan-3-yl ester(309253-79-0)
EPA Substance Registry System: Acetic acid (2R,3R,4R,5R)-4-acetoxy-5-acetoxymethyl-2-(6-phenylmethanesulfonyl-purin-9-yl)-tetrahydro-furan-3-yl ester(309253-79-0)

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: 309253-79-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 309253-79-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,9,2,5 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 309253-79:
(8*3)+(7*0)+(6*9)+(5*2)+(4*5)+(3*3)+(2*7)+(1*9)=140
140 % 10 = 0
So 309253-79-0 is a valid CAS Registry Number.

309253-79-0Upstream product

309253-79-0Downstream Products

23589-16-4 N₆-phenyladenosine

309253-79-0Relevant academic research and scientific papers

Mild and efficient functionalization at C6 of purine 2′-deoxynucleosides and ribonucleosides

Lin, Xiaoyu,Robins, Morris J.

, p. 3497 - 3499 (2000)

(Equation Presented) Treatment of sugar-protected inosine and 2′-deoxyinosine derivatives with a cyclic secondary amine or imidazole and I2/Ph3P/EtN(i-Pr)2/(CH2-Cl 2 or toluene) gave quantitative conversions into 6-N-(substituted)purine nucleosides. SNAr reactions with (imidazol-1-yl) derivatives gave 6-(N, O, or S)-substituted products. The 6-(benzylsulfonyl) group underwent SNAr displacement with an arylamine at ambient temperature.

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