Cas 439588-92-8,3-((E)-1-Methyl-3-triisopropylsilanyloxy-propenyl)-1-trimethylsilanyloxy-cyclohexene

439588-92-8

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Basic information

Product Name: 3-((E)-1-Methyl-3-triisopropylsilanyloxy-propenyl)-1-trimethylsilanyloxy-cyclohexene
Synonyms: 3-((E)-1-Methyl-3-triisopropylsilanyloxy-propenyl)-1-trimethylsilanyloxy-cyclohexene
CAS NO:439588-92-8
Molecular Formula:
Molecular Weight: 396.761
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: 3-((E)-1-Methyl-3-triisopropylsilanyloxy-propenyl)-1-trimethylsilanyloxy-cyclohexene(CAS DataBase Reference)
NIST Chemistry Reference: 3-((E)-1-Methyl-3-triisopropylsilanyloxy-propenyl)-1-trimethylsilanyloxy-cyclohexene(439588-92-8)
EPA Substance Registry System: 3-((E)-1-Methyl-3-triisopropylsilanyloxy-propenyl)-1-trimethylsilanyloxy-cyclohexene(439588-92-8)

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: 439588-92-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 439588-92-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,9,5,8 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 439588-92:
(8*4)+(7*3)+(6*9)+(5*5)+(4*8)+(3*8)+(2*9)+(1*2)=208
208 % 10 = 8
So 439588-92-8 is a valid CAS Registry Number.

439588-92-8Upstream product

439588-92-8Downstream Products

439588-92-8Relevant academic research and scientific papers

Synthetic studies of zoanthamine alkaloids. Stereoselective synthesis of the ABC ring system of norzoanthamine by an intramolecular Diels-Alder reaction

Sakai, Mio,Sasaki, Minoru,Tanino, Keiji,Miyashita, Masaaki

, p. 1705 - 1708 (2002)

Stereoselective synthesis of the ABC ring system of norzoanthamine having five asymmetric centers including two quaternary carbon atoms has been successfully accomplished by an intramolecular Diels-Alder reaction. A key intermediate for the Diels-Alder re

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