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26799-07-5

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26799-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26799-07-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,7,9 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 26799-07:
(7*2)+(6*6)+(5*7)+(4*9)+(3*9)+(2*0)+(1*7)=155
155 % 10 = 5
So 26799-07-5 is a valid CAS Registry Number.

26799-07-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Bis(phenylsilyl)methane

1.2 Other means of identification

Product number -
Other names (PhSiH2)2CH2

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:26799-07-5 SDS

26799-07-5Relevant academic research and scientific papers

Synthetic Pathways to Disilylmethane, H3SiCH2SiH3 and Methyldisilane, CH3SiH2SiH3

Zech, Joachim,Schmidbaur, Hubert

, p. 2087 - 2091 (2007/10/02)

Disilylmethane is available in a four-step synthesis starting with phenylsilane.This is converted into chlorophenylsilane by HCl/AlCl3.The reaction of PhSiH2Cl and bibromomethane with magnesium in tetrahydrofuran affords bis(phenylsilyl)methane, which yields bis(bromosilyl)methane by treatment with anhydrous hydrogen bromide. (BrH2Si)2CH2 is converted into disilylmethane by reduction with LiAlH4 in a two-phase system using a phase-transfer catalyst. - Methyldisilane is available by alkylation of monohalodisilane, XSi2H5 (X=Cr, Br), with methyllithium in a high-boiling ether or by silylation of bromomethylsilane with silylpotassium.Due to secondary silylation reactions the overall yields of methyldisilane are low in all cases.

A Synthetic Route to Poly(silyl)methanes via Poly(phenylsilyl)methanes and Poly(bromosilyl)methanes

Hager, Rudolf,Steigelmann, Oliver,Mueller, Gerhard,Schmidbaur, Hubert

, p. 2115 - 2120 (2007/10/02)

A three-step synthesis is presented for di- and tri(silyl)methane, two feedstock gases for the chemical vapour deposition of amorphous hydrogenated silicon/carbon alloys (a-SiC:H).Chloro(phenyl)silane and di-or trihalomethanes react with magnesium in tetrahydrofuran to give high yields of bis- and tris(phenylsilyl)methane, respectively.The two products can be converted into bis- and tris(bromosilyl)methane by treatment with anhydrous hydrogen bromide.Bromide/hydride substitution in these precursors is accomplished with lithium aluminum hydride in a two phase system using a phase-transfer catalyst.The compounds CH2(SiH2Ph)2, CH(SiH2Ph)3, CH2(SiH2Br)2, CH(SiH2Br)3, CH2(SiH3)2, and CH(SiH3)3 have been characterized by standard spectroscopic methods, and the crystal and molecular structure of CH(SiH2Ph)3 has been determined by single-crystal X-ray diffraction.The molecule adopts a conformation with crystallographic C3 symmetry.This result is discussed with regard to the structure of related molecules with three substituents of potential Cs symmetry at a tetrahedral center. - Key Words: CVD feedstock gases / Poly(bromosilyl)methanes / Poly(phenylsilyl)methanes / Poly(silyl)methanes / Silanes

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