Cas 341497-33-4,(R)-2-[6'-(tert-butyldiphenylsiloxy)-1'-cyclohexen-1'-yl]ethylamine

341497-33-4

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Basic information

Product Name: (R)-2-[6'-(tert-butyldiphenylsiloxy)-1'-cyclohexen-1'-yl]ethylamine
Synonyms: (R)-2-[6'-(tert-butyldiphenylsiloxy)-1'-cyclohexen-1'-yl]ethylamine
CAS NO:341497-33-4
Molecular Formula:
Molecular Weight: 379.618
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)-2-[6'-(tert-butyldiphenylsiloxy)-1'-cyclohexen-1'-yl]ethylamine(CAS DataBase Reference)
NIST Chemistry Reference: (R)-2-[6'-(tert-butyldiphenylsiloxy)-1'-cyclohexen-1'-yl]ethylamine(341497-33-4)
EPA Substance Registry System: (R)-2-[6'-(tert-butyldiphenylsiloxy)-1'-cyclohexen-1'-yl]ethylamine(341497-33-4)

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: 341497-33-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 341497-33-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,1,4,9 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 341497-33:
(8*3)+(7*4)+(6*1)+(5*4)+(4*9)+(3*7)+(2*3)+(1*3)=144
144 % 10 = 4
So 341497-33-4 is a valid CAS Registry Number.

341497-33-4Upstream product

252765-94-9 benzyl 2-[(6'R)-(tert-butyldiphenylsiloxy)cyclohex-1-enyl]ethylcarbamate

341497-33-4Downstream Products

341497-49-2 {2-[6-(tert-butyl-diphenyl-silanyloxy)-cyclohex-1-enyl]-ethyl}-(1-ethoxy-2-methyl-propyl)-carbamic acid ethyl ester

341497-33-4Relevant academic research and scientific papers

A new asymmetric synthesis of trans-hydroisoquinolones

Kamatani, Asayuki,Overman, Larry E.

, p. 1229 - 1232 (2001)

Matrix presented A convenient enantioselective synthesis of trans-hydroisoquinolones is described. This synthesis capitalizes on the ready availability of enantioenriched 2-substituted cyclohexenols by exploiting the asymmetry of an allylic carbon-oxygen

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