Cas 389798-87-2,trans-1,2,3,3-tetrakis(di-tert-butyl(methyl)silyl)-1-(1-phenylvinyloxy)disilagermirane

389798-87-2

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Basic information

Product Name: trans-1,2,3,3-tetrakis(di-tert-butyl(methyl)silyl)-1-(1-phenylvinyloxy)disilagermirane
Synonyms:
CAS NO:389798-87-2
Molecular Formula:
Molecular Weight: 878.317
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: trans-1,2,3,3-tetrakis(di-tert-butyl(methyl)silyl)-1-(1-phenylvinyloxy)disilagermirane(CAS DataBase Reference)
NIST Chemistry Reference: trans-1,2,3,3-tetrakis(di-tert-butyl(methyl)silyl)-1-(1-phenylvinyloxy)disilagermirane(389798-87-2)
EPA Substance Registry System: trans-1,2,3,3-tetrakis(di-tert-butyl(methyl)silyl)-1-(1-phenylvinyloxy)disilagermirane(389798-87-2)

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: 389798-87-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 389798-87-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,9,7,9 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 389798-87:
(8*3)+(7*8)+(6*9)+(5*7)+(4*9)+(3*8)+(2*8)+(1*7)=252
252 % 10 = 2
So 389798-87-2 is a valid CAS Registry Number.

389798-87-2Upstream product

389798-86-1 cis-1,2,3,3-tetrakis(di-tert-butyl(methyl)silyl)-1-(1-phenylvinyloxy)disilagermirane

389798-87-2Downstream Products

389798-87-2Relevant academic research and scientific papers

A new pathway in the reaction of disilene with carbonyl compounds: An 'ene' reaction instead of cycloaddition

Lee,Ichinohe,Sekiguchi

, p. 2146 - 2147 (2001)

The 3H-disilagermirene, (tBu2MeSi)4GeSi2, reacts with α-hydrogen containing carbonyl compounds (acetophenone, butane-2,3-dione) by an 'ene'-reaction pathway followed by isomerization or insertion reactions, representing a new mode in the reaction of disilenes with carbonyl compounds.

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