Cas 223708-55-2,1-(2-acetyl-5-O-benzyl-3-C-methylidene-3-deoxy-β-D-glycero-pentofuranosyl) thymine

223708-55-2

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Basic information

Product Name: 1-(2-acetyl-5-O-benzyl-3-C-methylidene-3-deoxy-β-D-glycero-pentofuranosyl) thymine
Synonyms: 1-(2-acetyl-5-O-benzyl-3-C-methylidene-3-deoxy-β-D-glycero-pentofuranosyl) thymine
CAS NO:223708-55-2
Molecular Formula:
Molecular Weight: 386.404
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: 1-(2-acetyl-5-O-benzyl-3-C-methylidene-3-deoxy-β-D-glycero-pentofuranosyl) thymine(CAS DataBase Reference)
NIST Chemistry Reference: 1-(2-acetyl-5-O-benzyl-3-C-methylidene-3-deoxy-β-D-glycero-pentofuranosyl) thymine(223708-55-2)
EPA Substance Registry System: 1-(2-acetyl-5-O-benzyl-3-C-methylidene-3-deoxy-β-D-glycero-pentofuranosyl) thymine(223708-55-2)

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: 223708-55-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 223708-55-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,7,0 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 223708-55:
(8*2)+(7*2)+(6*3)+(5*7)+(4*0)+(3*8)+(2*5)+(1*5)=122
122 % 10 = 2
So 223708-55-2 is a valid CAS Registry Number.

223708-55-2Upstream product

223708-55-2Downstream Products

223708-56-3 1-(5-O-benzyl-3-C-methylidene-3-deoxy-β-D-glycero-pentofuranosyl) thymine

223708-55-2Relevant academic research and scientific papers

Strategy for the preparation of 2' and 3' branched nucleosides

Len,Postel,Mackenzie,Villa,Ronco

, p. 165 - 168 (1999)

1-(5-O-Benzyl-3-C-methylidene-2-oxo-3-deoxy-β-D-glycero-pentofuranosyl) thymine was prepared as the precursor of 2',3'-dibranched nucleosides in six steps from 5-O-benzyl-1,2-O-isopropylidene-α-D-xylofuranose. This enone is the key starting compound for the preparation of a large series of potential antiretroviral agents against HIV-1.

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