Cas 170703-76-1,1,5-Bis-(dimethyl-phenyl-silanyl)-2,2,3,3,4,4,6,6-octamethyl-2,3,4,6-tetrasila-bicyclo[3.1.0]hexane

170703-76-1

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Basic information

Product Name: 1,5-Bis-(dimethyl-phenyl-silanyl)-2,2,3,3,4,4,6,6-octamethyl-2,3,4,6-tetrasila-bicyclo[3.1.0]hexane
Synonyms:
CAS NO:170703-76-1
Molecular Formula:
Molecular Weight: 527.164
EINECS: N/A
Product Categories: N/A
Mol File: 170703-76-1.mol
Article Data: 1

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: 1,5-Bis-(dimethyl-phenyl-silanyl)-2,2,3,3,4,4,6,6-octamethyl-2,3,4,6-tetrasila-bicyclo[3.1.0]hexane(CAS DataBase Reference)
NIST Chemistry Reference: 1,5-Bis-(dimethyl-phenyl-silanyl)-2,2,3,3,4,4,6,6-octamethyl-2,3,4,6-tetrasila-bicyclo[3.1.0]hexane(170703-76-1)
EPA Substance Registry System: 1,5-Bis-(dimethyl-phenyl-silanyl)-2,2,3,3,4,4,6,6-octamethyl-2,3,4,6-tetrasila-bicyclo[3.1.0]hexane(170703-76-1)

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: 170703-76-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 170703-76-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,7,0 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 170703-76:
(8*1)+(7*7)+(6*0)+(5*7)+(4*0)+(3*3)+(2*7)+(1*6)=121
121 % 10 = 1
So 170703-76-1 is a valid CAS Registry Number.

170703-76-1Upstream product

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170703-76-1Relevant articles and documents

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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