Cas 136292-95-0,(3R,4R)-3-(tert-Butoxy-dimethyl-silanyl)-3,4-bis-(dimethyl-phenyl-silanyl)-1,1,2,2-tetramethyl-[1,2]disiletane

136292-95-0

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Basic information

Product Name: (3R,4R)-3-(tert-Butoxy-dimethyl-silanyl)-3,4-bis-(dimethyl-phenyl-silanyl)-1,1,2,2-tetramethyl-[1,2]disiletane
Synonyms:
CAS NO:136292-95-0
Molecular Formula:
Molecular Weight: 543.132
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: (3R,4R)-3-(tert-Butoxy-dimethyl-silanyl)-3,4-bis-(dimethyl-phenyl-silanyl)-1,1,2,2-tetramethyl-[1,2]disiletane(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4R)-3-(tert-Butoxy-dimethyl-silanyl)-3,4-bis-(dimethyl-phenyl-silanyl)-1,1,2,2-tetramethyl-[1,2]disiletane(136292-95-0)
EPA Substance Registry System: (3R,4R)-3-(tert-Butoxy-dimethyl-silanyl)-3,4-bis-(dimethyl-phenyl-silanyl)-1,1,2,2-tetramethyl-[1,2]disiletane(136292-95-0)

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: 136292-95-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 136292-95-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,2,9 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 136292-95:
(8*1)+(7*3)+(6*6)+(5*2)+(4*9)+(3*2)+(2*9)+(1*5)=140
140 % 10 = 0
So 136292-95-0 is a valid CAS Registry Number.

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136292-95-0Relevant academic research and scientific papers

Decomposition of bis( silyldiazomethyl) polysilanes: formation of polysilabicyclo(l.m.n)alkane derivatives

Ando, Wataru,Sugiyama, Mitsuru,Suzuki, Tomohisa,Kato, Chikako,Arakawa, Yusuke,Kabe, Yoshio

, p. 99 - 112 (2007/10/02)

The photolysis of bis(trimethylsilyldiazomethyl)disilane (4a) in tert-butyl alcohol provided the tert-butyl alcohol adducts S, 6, 7, 8 and 9.The structures of these products revealed the stepwise formation of asymmetric silenes as intermediates.Gas-phase

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