Cas 183279-94-9,1-(3-O-tert-butyldiphenylsilyl-2,5-dideoxy-β-D-glycero-pent-4-enofuranosyl)thymine

183279-94-9

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Basic information

Product Name: 1-(3-O-tert-butyldiphenylsilyl-2,5-dideoxy-β-D-glycero-pent-4-enofuranosyl)thymine
Synonyms: 1-(3-O-tert-butyldiphenylsilyl-2,5-dideoxy-β-D-glycero-pent-4-enofuranosyl)thymine
CAS NO:183279-94-9
Molecular Formula:
Molecular Weight: 462.621
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-(3-O-tert-butyldiphenylsilyl-2,5-dideoxy-β-D-glycero-pent-4-enofuranosyl)thymine(CAS DataBase Reference)
NIST Chemistry Reference: 1-(3-O-tert-butyldiphenylsilyl-2,5-dideoxy-β-D-glycero-pent-4-enofuranosyl)thymine(183279-94-9)
EPA Substance Registry System: 1-(3-O-tert-butyldiphenylsilyl-2,5-dideoxy-β-D-glycero-pent-4-enofuranosyl)thymine(183279-94-9)

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: 183279-94-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 183279-94-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,2,7 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 183279-94:
(8*1)+(7*8)+(6*3)+(5*2)+(4*7)+(3*9)+(2*9)+(1*4)=169
169 % 10 = 9
So 183279-94-9 is a valid CAS Registry Number.

183279-94-9Upstream product

183279-94-9Downstream Products

183280-00-4 dimethyl (3-O-tert-butyldiphenylsilyl-5-iodo-1-thymin-1-yl-1,2,5-trideoxy-β-D-erythro-pentofuranos-4-yloxy)methylphosphonate

183279-94-9Relevant academic research and scientific papers

Nucleoside 5′-C-phosphonates: reactivity of the α-hydroxyphosphonate moiety

Králíková, ?árka,Budě?ínky, Milo?,Masojídková, Milena,Rosenberg, Ivan

, p. 4917 - 4932 (2007/10/03)

We found that various dialkyl phosphites, dialkyl trimethylsilyl phosphites, and tris-trimethylsilyl phosphite reacted smoothly with nucleoside 5′-aldehydes to afford epimeric nucleoside 5′-C-phosphonates in high yields. A number of these compounds in bot

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