Cas 1173294-00-2,(2S,3S,4S)-5-bromo-1-(methyldiphenylsilyl)-2,3,4-(trimethoxy)pentan-1-one

1173294-00-2

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Basic information

Product Name: (2S,3S,4S)-5-bromo-1-(methyldiphenylsilyl)-2,3,4-(trimethoxy)pentan-1-one
Synonyms: (2S,3S,4S)-5-bromo-1-(methyldiphenylsilyl)-2,3,4-(trimethoxy)pentan-1-one
CAS NO:1173294-00-2
Molecular Formula:
Molecular Weight: 451.432
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: (2S,3S,4S)-5-bromo-1-(methyldiphenylsilyl)-2,3,4-(trimethoxy)pentan-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S,4S)-5-bromo-1-(methyldiphenylsilyl)-2,3,4-(trimethoxy)pentan-1-one(1173294-00-2)
EPA Substance Registry System: (2S,3S,4S)-5-bromo-1-(methyldiphenylsilyl)-2,3,4-(trimethoxy)pentan-1-one(1173294-00-2)

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: 1173294-00-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1173294-00-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,3,2,9 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1173294-00:
(9*1)+(8*1)+(7*7)+(6*3)+(5*2)+(4*9)+(3*4)+(2*0)+(1*0)=142
142 % 10 = 2
So 1173294-00-2 is a valid CAS Registry Number.

1173294-00-2Upstream product

1173293-90-7 C₂₂H₃₀O₇SSi

1173294-00-2Downstream Products

1173293-91-8 C₂₁H₂₈O₄Si

1173294-00-2Relevant academic research and scientific papers

The synthesis of carbohydrate-derived acylsilanes and their intramolecular free radical cyclizations with the formation of polyoxygenated cyclopentanes

Chang, Che-Chien,Kuo, Yu-Hsien,Tsai, Yeun-Min

scheme or table, p. 3805 - 3808 (2009/10/11)

A convenient way for the synthesis of acylsilanes from arabinose, lyxose, and ribose is developed. All the chiral centers of the carbohydrate templates are conserved, and only the reducing end is transformed into the acylsilane functional group. The non-r

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