Cas 1108203-24-2,(R,E)-3-(4-(tert-butyldimethylsilyloxy)but-2-enoyl)-4-isopropyl-5,5-diphenyloxazolidin-2-one

1108203-24-2

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Basic information

Product Name: (R,E)-3-(4-(tert-butyldimethylsilyloxy)but-2-enoyl)-4-isopropyl-5,5-diphenyloxazolidin-2-one
Synonyms: (R,E)-3-(4-(tert-butyldimethylsilyloxy)but-2-enoyl)-4-isopropyl-5,5-diphenyloxazolidin-2-one
CAS NO:1108203-24-2
Molecular Formula:
Molecular Weight: 479.692
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: (R,E)-3-(4-(tert-butyldimethylsilyloxy)but-2-enoyl)-4-isopropyl-5,5-diphenyloxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (R,E)-3-(4-(tert-butyldimethylsilyloxy)but-2-enoyl)-4-isopropyl-5,5-diphenyloxazolidin-2-one(1108203-24-2)
EPA Substance Registry System: (R,E)-3-(4-(tert-butyldimethylsilyloxy)but-2-enoyl)-4-isopropyl-5,5-diphenyloxazolidin-2-one(1108203-24-2)

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: 1108203-24-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1108203-24-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,8,2,0 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1108203-24:
(9*1)+(8*1)+(7*0)+(6*8)+(5*2)+(4*0)+(3*3)+(2*2)+(1*4)=92
92 % 10 = 2
So 1108203-24-2 is a valid CAS Registry Number.

1108203-24-2Upstream product

191090-32-1 (R)-4-(1-methylethyl)-5,5-diphenyl-1,3-oxazolidin-2-one

1108203-24-2Downstream Products

1108203-25-3 (R)-3-((1R,6R)-6-((tert-butyldimethylsilyloxy)methyl)-4-methylcyclohex-3-enecarbonyl)-4-isopropyl-5,5-diphenyloxazolidin-2-one

1108203-24-2Relevant academic research and scientific papers

A rapid, asymmetric synthesis of the decahydrofluorene core of the hirsutellones

Tilley, S. David,Reber, Keith P.,Sorensen, Erik J.

supporting information; experimental part, p. 701 - 703 (2009/08/14)

(Chemical Equation Presented) A tandem ketene-trapping/Diels-Alder cyclization sequence was the pivotal transformation in an efficient, asymmetric synthesis of a decahydrofluorene tricyclic structure possessing eight stereogenic centers and key features o

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