Cas 150423-39-5,(1S,4R,5S,6R)-5,6-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-bicyclo[2.2.1]hept-2-ene

150423-39-5

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Basic information

Product Name: (1S,4R,5S,6R)-5,6-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-bicyclo[2.2.1]hept-2-ene
Synonyms:
CAS NO:150423-39-5
Molecular Formula:
Molecular Weight: 631.018
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: (1S,4R,5S,6R)-5,6-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-bicyclo[2.2.1]hept-2-ene(CAS DataBase Reference)
NIST Chemistry Reference: (1S,4R,5S,6R)-5,6-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-bicyclo[2.2.1]hept-2-ene(150423-39-5)
EPA Substance Registry System: (1S,4R,5S,6R)-5,6-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-bicyclo[2.2.1]hept-2-ene(150423-39-5)

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: 150423-39-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 150423-39-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,4,2 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 150423-39:
(8*1)+(7*5)+(6*0)+(5*4)+(4*2)+(3*3)+(2*3)+(1*9)=95
95 % 10 = 5
So 150423-39-5 is a valid CAS Registry Number.

150423-39-5Upstream product

150423-39-5Downstream Products

150423-40-8 (1R,4S,5R,6S)-5,6-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-bicyclo[2.2.1]heptane-2,3-dione

150423-39-5Relevant academic research and scientific papers

Differentiation of enantiotopic carbonyl groups by the Horner-Wadsworth-Emmons reaction

Tanaka,Ohta,Fuji,Taga

, p. 4071 - 4074 (1993)

A chiral phosphonoacetate 2 differentiates the enantiotopic carbonyl groups in an α-diketones 5 to afford the Z-olefin 6 in high yield and ee. The absolute stereochemistry of 6 was determined by X-ray analysis of 8 derived from 6.

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