Cas 126210-38-6,1-(2,6-diisopropylphenyl)-2,2,4,4-tetramethyl-3,3-bis(trimethylsilyl)-1-aza-2,4-disilacyclobutane

126210-38-6

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Basic information

Product Name: 1-(2,6-diisopropylphenyl)-2,2,4,4-tetramethyl-3,3-bis(trimethylsilyl)-1-aza-2,4-disilacyclobutane
Synonyms: 1-(2,6-diisopropylphenyl)-2,2,4,4-tetramethyl-3,3-bis(trimethylsilyl)-1-aza-2,4-disilacyclobutane
CAS NO:126210-38-6
Molecular Formula:
Molecular Weight: 449.975
EINECS: N/A
Product Categories: N/A
Mol File: 126210-38-6.mol
Article Data: 2

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-(2,6-diisopropylphenyl)-2,2,4,4-tetramethyl-3,3-bis(trimethylsilyl)-1-aza-2,4-disilacyclobutane(CAS DataBase Reference)
NIST Chemistry Reference: 1-(2,6-diisopropylphenyl)-2,2,4,4-tetramethyl-3,3-bis(trimethylsilyl)-1-aza-2,4-disilacyclobutane(126210-38-6)
EPA Substance Registry System: 1-(2,6-diisopropylphenyl)-2,2,4,4-tetramethyl-3,3-bis(trimethylsilyl)-1-aza-2,4-disilacyclobutane(126210-38-6)

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: 126210-38-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 126210-38-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,2,1 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 126210-38:
(8*1)+(7*2)+(6*6)+(5*2)+(4*1)+(3*0)+(2*3)+(1*8)=86
86 % 10 = 6
So 126210-38-6 is a valid CAS Registry Number.

126210-38-6Upstream product

126210-38-6Downstream Products

126210-38-6Relevant articles and documents

Palladium-catalyzed insertion of isocyanides into the silicon-silicon linkages of oligosilanes

Ito, Yoshihiko,Suginome, Michinori,Matsuura, Takaharu,Murakami, Masahiro

, p. 8899 - 8908 (2007/10/02)

Full details of a study on the reactions of oligosilanes with isocyanides promoted by a palladium catalyst are described. Heating a mixture of oligosilanes and excess 2,6-disubstituted aryl isocyanide in the presence of palladium(II) acetate led to the co

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