Cas 272778-75-3,5'-O-tert-butyldiphenylsilyl-3'-O<sup>2</sup>-[(4-dimethylamino-4-methyl)-1,3-thiazol-2-inyl]-thymidine

272778-75-3

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Basic information

Product Name: 5'-O-tert-butyldiphenylsilyl-3'-O²-[(4-dimethylamino-4-methyl)-1,3-thiazol-2-inyl]-thymidine
Synonyms: 5'-O-tert-butyldiphenylsilyl-3'-O²-[(4-dimethylamino-4-methyl)-1,3-thiazol-2-inyl]-thymidine
CAS NO:272778-75-3
Molecular Formula:
Molecular Weight: 622.861
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: 5'-O-tert-butyldiphenylsilyl-3'-O²-[(4-dimethylamino-4-methyl)-1,3-thiazol-2-inyl]-thymidine(CAS DataBase Reference)
NIST Chemistry Reference: 5'-O-tert-butyldiphenylsilyl-3'-O²-[(4-dimethylamino-4-methyl)-1,3-thiazol-2-inyl]-thymidine(272778-75-3)
EPA Substance Registry System: 5'-O-tert-butyldiphenylsilyl-3'-O²-[(4-dimethylamino-4-methyl)-1,3-thiazol-2-inyl]-thymidine(272778-75-3)

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: 272778-75-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 272778-75-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,2,7,7 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 272778-75:
(8*2)+(7*7)+(6*2)+(5*7)+(4*7)+(3*8)+(2*7)+(1*5)=183
183 % 10 = 3
So 272778-75-3 is a valid CAS Registry Number.

272778-75-3Upstream product

1774-47-6 trimethylsulfoxonium iodide

272778-75-3Downstream Products

272778-75-3Relevant academic research and scientific papers

Synthesis of 3'-O2-(azaheterocycle)-thymidines.

Prestat,Dubreuil,Adjou,Pradere,Lebreton,Evers,Henin

, p. 735 - 748 (2000)

The synthesis of 3'-O2-(azaheterocycle)-thymidines is presented from 1-thia-3-aza- 1,3-butadiene precursors (N-thioacylamidines). A variety of heterocycles is accessible using the dienic, the electrophilic or the nucleophilic reactivity of these thia-azab

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