Cas 849518-88-3,Silanamine, N-(cyclopentylphenylethenylidene)-1-(1,1-dimethylethyl)-1,1-dimethyl-

849518-88-3

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Basic information

Product Name: Silanamine, N-(cyclopentylphenylethenylidene)-1-(1,1-dimethylethyl)-1,1-dimethyl-
Synonyms:
CAS NO:849518-88-3
Molecular Formula: C19H29NSi
Molecular Weight: 299.531
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: Silanamine, N-(cyclopentylphenylethenylidene)-1-(1,1-dimethylethyl)-1,1-dimethyl-(CAS DataBase Reference)
NIST Chemistry Reference: Silanamine, N-(cyclopentylphenylethenylidene)-1-(1,1-dimethylethyl)-1,1-dimethyl-(849518-88-3)
EPA Substance Registry System: Silanamine, N-(cyclopentylphenylethenylidene)-1-(1,1-dimethylethyl)-1,1-dimethyl-(849518-88-3)

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: 849518-88-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 849518-88-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,5,1 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 849518-88:
(8*8)+(7*4)+(6*9)+(5*5)+(4*1)+(3*8)+(2*8)+(1*8)=223
223 % 10 = 3
So 849518-88-3 is a valid CAS Registry Number.

849518-88-3Upstream product

140-29-4 phenylacetonitrile

849518-88-3Downstream Products

849518-88-3Relevant academic research and scientific papers

Nucleophile-catalyzed asymmetric acylations of silyl ketene imines: Application to the enantioselective synthesis of verapamil

Mermerian, Ara H.,Fu, Gregory C.

, p. 949 - 952 (2005)

All-carbon quaternary stereocenters are generated with good enantioselectivity through a nucleophile-catalyzed acylation reaction of silyl ketene imines (see scheme, TBS = tert-butyldimethylsilyl). The method is applied to the first catalytic asymmetric synthesis of the drug verapamil.

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