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Silane, chloro(chloromethyl)methylphenyl-, also known as (chloromethyl)(chloromethyl)phenylsilane or 1,1,1-trichloro-2-phenylsilapropane, is an organosilicon compound with the chemical formula C9H10Cl3Si. It is a colorless liquid with a molecular weight of 259.62 g/mol. Silane, chloro(chloromethyl)methylphenyl- is characterized by the presence of a phenyl group attached to a silicon atom, which is further bonded to two chloromethyl groups and one chlorine atom. Silane, chloro(chloromethyl)methylphenyl-, is primarily used as a coupling agent in the production of composite materials, particularly in the reinforcement of plastics and rubber with fillers such as glass fibers. It enhances the adhesion between the filler and the matrix, improving the mechanical properties and durability of the final product. Due to its reactivity, it is essential to handle Silane, chloro(chloromethyl)methylphenyl- with care, following proper safety protocols.

2632-83-9

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2632-83-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2632-83-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,3 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2632-83:
(6*2)+(5*6)+(4*3)+(3*2)+(2*8)+(1*3)=79
79 % 10 = 9
So 2632-83-9 is a valid CAS Registry Number.

2632-83-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name chloro(chloromethyl)(methyl)phenylsilane

1.2 Other means of identification

Product number -
Other names Chlor-chlormethyl-methyl-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:2632-83-9 SDS

2632-83-9Relevant academic research and scientific papers

Palladium-Catalyzed β-Elimination of Aminoboranes from (Aminomethylsilyl)boranes Leading to the Formation of Silene Dimers

Ohmura, Toshimichi,Nishiura, Hiroki,Suginome, Michinori

supporting information, p. 4298 - 4304 (2017/11/20)

Silylboronic esters bearing a N,N-dialkylaminomethyl group on the silicon atoms were synthesized and used in palladium-catalyzed reactions. Five silylboronic esters were synthesized through a reaction of the [(N,N-dialkylaminomethyl)diorganosilyl]lithiums

Preparation of sila-functional 3-sila-1-thiacyclohexanes

Kirpichenko, Svetlana V.,Albanov, Aleksander I.

experimental part, p. 663 - 666 (2010/04/24)

First sila-functional heterocycles 7 and 9 with Si and S atoms in 1,3-position bearing the reactive X group at silicon (X = i-PrO, F) were readily prepared from the corresponding phenyl-protected cycle 6 in good yields via Ph-Si bond cleavage by electroph

Highly diastereoselective intramolecular Diels-Alder reaction of chiral silatrienes

Coelho, Paulo J.,Blanco, Luis

, p. 2451 - 2456 (2007/10/03)

New Si-chiral 2-silahexa-3,5-dienyl acrylates were prepared in six steps from dichloro(chloromethyl)methylsilane. The EtAlCl2 catalysed intramolecular Diels-Alder reaction of these compounds gave chiral 4-sila-4a,7,8,8a-tetrahydroisochroman-1-ones in good yield. Very good diastereoselectivity was observed for a silatriene bearing a methyl and a 2-methoxyphenyl substituent on the chiral silicon atom.

Diastereoselective synthesis of 4-sila-3,4,4a,5-tetrahydro-2H-isoquinolin-1-ones through intramolecular Diels-Alder reaction of chiral silatrienes

Coelho,Blanco

, p. 1455 - 1457 (2007/10/03)

New Si-chiral N-2-silabut-3-enylpyran-2-one-6carboxamides were prepared in four steps from dichloro(chloro-methyl)methylsilane. The thermal inverse electron demand intra-molecular Diels-Alder reaction of these compounds gave 4-sila3,4,4a,5-tetrahydro-2H-isoquinolin-1-ones. Moderate diastereoselectivity was observed for a silatriene bearing a methyl and a cyclohexyl substituent on the chiral silicon atom. The intermediate tricyclic adduct of this reaction was also isolated.

Fungicidal 1,2,4-triazole derivatives

-

, (2008/06/13)

Silicon-containing 1,2,4-triazoles having broad-spectrum fungicidal activity have been discovered.

Fungicidal imidazole derivatives

-

, (2008/06/13)

Silicon-containing imidazoles having broad-spectrum fungicidal activity have been discovered.

Synthesis and Properties of (Hydroxymethyl)diorganylsilanes

Tacke, Reinhold,Lange, Hartwig,Bentlage, Anke

, p. 3673 - 3677 (2007/10/02)

The synthesis of the (hydroxymethyl)diorganylsilanes R1R2Si(H)CH2OH (4a: R1 = R2 = CH3, 2-silaisobutanol; 4b: R1 = CH3, R2 = C6H5; 4c: R1 = R2 = C6H5) is achieved by the reaction of R1R2Si(Cl)CH2Cl (2a - c) with AcOH/NEt3 to R1R2Si(OAc)CH2OAc (3a - c), fo

SILAETHENE II. DARSTELLUNG UND CHARAKTERISIERUNG VON 1,3-DISILACYCLOBUTANEN

Auner, N.,Grobe, J.

, p. 151 - 178 (2007/10/02)

1,3-Disilacyclobutanes of the types R1R2SiSiR1R2 are prepared (a) by ring synthesis from chloromethylchlorosilanes R1R2Si(CH2Cl)Cl, (b) by thermolysis of monosilacyclobutanes , and (c) by substitution of chlorine with alkyl groups in SiCl-containing 1,3-disilacyclobutanes, obtained by procedures (a) or (b).The compounds have been characterized by analytical and spectroscopic investigations.The synthetic methods are critically compared.

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