Cas 944148-97-4,2',3'-O-isopropylidene-5'-O-trityl-4-O-[(2,4,6-triisopropylbenzene)sulfonyl]uridine

944148-97-4

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Basic information

Product Name: 2',3'-O-isopropylidene-5'-O-trityl-4-O-[(2,4,6-triisopropylbenzene)sulfonyl]uridine
Synonyms: 2',3'-O-isopropylidene-5'-O-trityl-4-O-[(2,4,6-triisopropylbenzene)sulfonyl]uridine
CAS NO:944148-97-4
Molecular Formula:
Molecular Weight: 792.993
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: 2',3'-O-isopropylidene-5'-O-trityl-4-O-[(2,4,6-triisopropylbenzene)sulfonyl]uridine(CAS DataBase Reference)
NIST Chemistry Reference: 2',3'-O-isopropylidene-5'-O-trityl-4-O-[(2,4,6-triisopropylbenzene)sulfonyl]uridine(944148-97-4)
EPA Substance Registry System: 2',3'-O-isopropylidene-5'-O-trityl-4-O-[(2,4,6-triisopropylbenzene)sulfonyl]uridine(944148-97-4)

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: 944148-97-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 944148-97-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,4,1,4 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 944148-97:
(8*9)+(7*4)+(6*4)+(5*1)+(4*4)+(3*8)+(2*9)+(1*7)=194
194 % 10 = 4
So 944148-97-4 is a valid CAS Registry Number.

944148-97-4Upstream product

944148-97-4Downstream Products

944148-97-4Relevant academic research and scientific papers

A general route to 4-C-substituted pyrimidine nucleosides

Hennecke, Ulrich,Kuch, David,Carell, Thomas

, p. 929 - 935 (2007)

Palladium-catalyzed cross-coupling reactions of tin and zinc nucleophiles with arylsulfonates of pyrimidine nucleosides have been achieved to give a wide range of 4-C-substituted pyrimidine nucleosides. This method also allows the construction of pyrimidi

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