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Silane, also known as SiH4, is a colorless, flammable, and toxic gas with a strong, unpleasant odor. It is a derivative of silicon, where each silicon atom is bonded to four hydrogen atoms. Bromophenyl, on the other hand, refers to a group of organic compounds consisting of a benzene ring with one or more bromine atoms attached to it. These compounds are used in various applications, such as pharmaceuticals, dyes, and pesticides. Both silane and bromophenyl are important in the field of chemistry, with silane being a precursor to various silicon-based materials and bromophenyl being a versatile building block for the synthesis of various organic compounds.

1631-90-9

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1631-90-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1631-90-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,3 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1631-90:
(6*1)+(5*6)+(4*3)+(3*1)+(2*9)+(1*0)=69
69 % 10 = 9
So 1631-90-9 is a valid CAS Registry Number.

1631-90-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name bromo-phenyl-silane

1.2 Other means of identification

Product number -
Other names Brom-phenyl-silan

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:1631-90-9 SDS

1631-90-9Upstream product

1631-90-9Relevant academic research and scientific papers

Selective synthesis of halosilanes from hydrosilanes and utilization for organic synthesis

Kunai, Atsutaka,Ohshita, Joji

, p. 3 - 15 (2007/10/03)

Selective synthesis of halosilanes has been examined. Various types of halosilanes and halohydrosilanes, such as R3SiX, R2SiHX, R2SiX2, RSiH2X, RSiHX2 (X=Cl, Br, F), were obtained by the reactions of the corresponding hydrosilanes with Cu(II)-based reagents selectively in high yields. This method could be also applied to the synthesis of chlorofluorosilanes and chlorohydrogermanes. On the other hand, iodo- and bromosilanes and germanes were obtained by Pd- or Ni-catalyzed hydride-halogen exchange reactions of hydrosilanes with alkyl or allyl halides. Their synthetic applications have been demonstrated by using iodo- and bromosilanes and chlorofluorosilanes.

Synthesis of bromohydrosilanes: Reactions of hydrosilanes with CuBr2 in the presence of CuI

Kunai, Atsutaka,Ochi, Takahiko,Iwata, Arihiro,Ohshita, Joji

, p. 1228 - 1229 (2007/10/03)

Reactions of hydrosilanes, R4-nSiHn (R = alkyl or phenyl, n = 1-3), with 2 equiv of CuBr2 in the presence of a catalytic amount of CuI led to selective replacement of an H-Si bond with a Br-Si bond giving R3SiBr, R2SiHBr, or RSiH2Br, while treatment of R2SiH2 and RSiH3 with 4 equiv of the reagent produced R2SiBr2 and RSiHBr2, respectively. Similar reaction of HEt2SiSiEt2H afforded HEt2SiSiEt2Br.

The Mechanism of the Reaction of Molecular Bromine with Organosilicon Hydrides

El-Durini, Nabil M. K.,Jackson, Richard A.

, p. 1275 - 1278 (2007/10/02)

The kinetics of the bromination of 7 triarylsilanes and 14 other organosilicon hydrides by molecular bromine in CCl4 have been determined by the stopped flow method.For triethylsilane, Arrhenius parameters have been measured in octane and CCl4, and solvent effects determined in other solvents of different polarity.The results accord with a molecular mechanism involving one molecule of bromine and one of the organosilicon hydride, with partial positive charge build-up on silicon in the transition state.

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