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Merck

440272

Dichlorodimethylsilane

≥99.5%

Synonym(s):

DMDCS, Dimethyldichlorosilane

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About This Item

Linear Formula:
(CH3)2SiCl2
CAS Number:
75-78-5
Molecular Weight:
129.06
UNSPSC Code:
12352103
NACRES:
NA.22
PubChem Substance ID:
24867582
EC Number:
200-901-0
Beilstein/REAXYS Number:
605287
MDL number:
MFCD00000491
Assay:
≥99.5%
Form:
liquid

Key Documents

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InChI key

LIKFHECYJZWXFJ-UHFFFAOYSA-N

InChI

1S/C2H6Cl2Si/c1-5(2,3)4/h1-2H3

SMILES string

C[Si](C)(Cl)Cl

assay

≥99.5%

form

liquid

Quality Level

200

bp

70 °C (lit.)

mp

−76 °C (lit.)

storage temp.

2-8°C

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Application

Common reagent for synthesis of optically active ansa-mettallocene polymerization catalysts.
Used to prepare a resin bound siloxane with reactivity towards tertiary alcohols.

Packaging

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signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

33.8 °F - closed cup

flash_point_c

1 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
SHBS0017
SHBR1788
SHBP6374
SHBN0421
SHBL9313

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Tetrahedron, 63, 299-299 (2007)
Cliff R Baar et al.
Journal of the American Chemical Society, 126(26), 8216-8231 (2004-07-01)
A series of enantiopure C1-symmetric metallocenes, [(SiMe2)2[eta5-C5H(CHMe2)2][eta5-C5H2((S)-CHMeCMe3)]]ZrCl2, (S)-2, [(SiMe2)2[eta5-C5H(CHEt2)2][eta5-C5H2((S)-CHMeCMe3)]]ZrCl2, (S)-6, and [(SiMe2)2[eta5-C5HCy2][eta5-C5H2((S)-CHMeCMe3)]]ZrCl2, (S)-7 (Cy = cyclohexyl), zirconocene dichlorides that have an enantiopure methylneopentyl substituent on the "upper" cyclopentadienyl ligand, and diastereomerically pure precatalysts, [(SiMe2)2[eta5-C5H((S)-CHMeCy)(CHMe2)][eta5-C5H3]]ZrCl2, (S)-8a and (S)-8b, which have an
Niels P Boks et al.
Microbiology (Reading, England), 154(Pt 10), 3122-3133 (2008-10-04)
Using a parallel-plate flow chamber, the hydrodynamic shear forces to prevent bacterial adhesion (F(prev)) and to detach adhering bacteria (F(det)) were evaluated for hydrophilic glass, hydrophobic, dimethyldichlorosilane (DDS)-coated glass and six different bacterial strains, in order to test the following
J M Curran et al.
Biomaterials, 32(21), 4753-4760 (2011-04-15)
Material modifications can be used to induce cell responses, in particular-CH(3) and -NH(2) have shown potential in enhancing the ability of a material to support mesenchymal stem cell (MSC) adhesion and differentiation. Currently this process is variable, due to the
R Bos et al.
Microbiology (Reading, England), 142 ( Pt 9), 2355-2361 (1996-09-01)
Co-adhesion between oral microbial pairs (i.e. adhesion of a planktonic microorganism to a sessile organism adhering to a substratum surface) has been described as a highly specific interaction, mediated by stereochemical groups on the interacting microbial cell surfaces, and also
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