Cas 234083-61-5,benzyl 4,6-di-O-benzoyl-2,3-dideoxy-2,2-difluoro-β-D-erythro-hexopyranoside

234083-61-5

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Basic information

Product Name: benzyl 4,6-di-O-benzoyl-2,3-dideoxy-2,2-difluoro-β-D-erythro-hexopyranoside
Synonyms: benzyl 4,6-di-O-benzoyl-2,3-dideoxy-2,2-difluoro-β-D-erythro-hexopyranoside
CAS NO:234083-61-5
Molecular Formula:
Molecular Weight: 482.481
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: benzyl 4,6-di-O-benzoyl-2,3-dideoxy-2,2-difluoro-β-D-erythro-hexopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: benzyl 4,6-di-O-benzoyl-2,3-dideoxy-2,2-difluoro-β-D-erythro-hexopyranoside(234083-61-5)
EPA Substance Registry System: benzyl 4,6-di-O-benzoyl-2,3-dideoxy-2,2-difluoro-β-D-erythro-hexopyranoside(234083-61-5)

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: 234083-61-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 234083-61-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,4,0,8 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 234083-61:
(8*2)+(7*3)+(6*4)+(5*0)+(4*8)+(3*3)+(2*6)+(1*1)=115
115 % 10 = 5
So 234083-61-5 is a valid CAS Registry Number.

234083-61-5Upstream product

98-88-4 benzoyl chloride

234083-61-5Downstream Products

234083-61-5Relevant academic research and scientific papers

Synthesis of 2',3'-dideoxy-3',3'-difluoro and 2',3'-dideoxy-2',2'- difluoro-pyranosyl nucleosides analogues of gemcitabine

Fernandez, Raul,Castillon, Sergio

, p. 8497 - 8508 (1999)

The gem-difluoronucleosides 1 and 2, pyranosyl analogues of gemcitabine, have been synthesized from D-mannose and D-glucose respectively. The key steps were the formation of the difluoromethylene group by reaction of the corresponding ulose with DAST, and the glycosylation.

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