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Sigma-Aldrich

Dimethylphenylsilane

≥98%

Synonym(s):

Phenyldimethylsilane

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About This Item

Linear Formula:
C6H5SiH(CH3)2
CAS Number:
766-77-8
Molecular Weight:
136.27
Beilstein:
2204906
EC Number:
212-170-5
MDL number:
MFCD00008257
UNSPSC Code:
12352103
PubChem Substance ID:
24854073
NACRES:
NA.22

Assay

≥98%

form

liquid

refractive index

n20/D 1.497 (lit.)

bp

157 °C/744 mmHg (lit.)

density

0.889 g/mL at 25 °C (lit.)

SMILES string

C[SiH](C)c1ccccc1

InChI

1S/C8H12Si/c1-9(2)8-6-4-3-5-7-8/h3-7,9H,1-2H3

InChI key

ZISUALSZTAEPJH-UHFFFAOYSA-N

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General description

Dimethylphenylsilane is used as a silylating agent in homocoupling reactions to produce well defined polymers.

Application

Reagent for enol ether synthesis.

Pictograms

Flame
GHS02

Signal Word

Warning

Hazard Statements

H226

Hazard Classifications

Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

95.0 °F

Flash Point(C)

35 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Diethylsilane 99%

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Cu3 (BTC) 2 catalyzed dehydrogenative coupling of dimethylphenylsilane with phenol and homocoupling of dimethylphenylsilane to disiloxane
Anbu, Nagaraj, et,al
Journal of Colloid and Interface Science, 490, 430-435 (2017)
B (C 6 F 5) 3-catalyzed group transfer polymerization of alkyl methacrylates with dimethylphenylsilane through in situ formation of silyl ketene acetal by B (C 6 F 5) 3-catalyzed 1, 4-hydrosilylation of methacrylate monomer
Chen, Yougen and Kitano
Open Journal of Polymer Chemistry, 6, 3502-3511 (2015)
Slawomir Rubinsztajn et al.
Macromolecular rapid communications, 42(5), e2000601-e2000601 (2020-12-04)
The reaction of poly(hydromethylsiloxane-co-methylphenylsiloxane) with zirconium (IV) n-propoxide in dry toluene leads to extensive scission of the siloxane chain and conversion of Si-H groups. These processes produce oligomeric siloxanes and organosilanes containing moisture sensitive propoxy and siloxy-zirconate groups. The obtained

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