80430
Dichlorodimethylsilane
Wacker Chemie AG, ≥99.0% (GC)
Synonym(s):
Silane M2, DMDCS, Dimethyldichlorosilane
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About This Item
Linear Formula:
(CH3)2SiCl2
CAS Number:
Molecular Weight:
129.06
UNSPSC Code:
12352101
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-901-0
Beilstein/REAXYS Number:
605287
MDL number:
Assay:
≥99.0% (GC)
Form:
liquid
Quality Level
assay
≥99.0% (GC)
form
liquid
manufacturer/tradename
Wacker Chemie AG
refractive index
n20/D 1.404 (lit.)
bp
70 °C (lit.)
mp
−76 °C (lit.)
density
1.07 g/mL at 25 °C (lit.)
SMILES string
C[Si](C)(Cl)Cl
InChI
1S/C2H6Cl2Si/c1-5(2,3)4/h1-2H3
InChI key
LIKFHECYJZWXFJ-UHFFFAOYSA-N
General description
Dichlorodimethylsilane is an organosilicon compound generally used as a protecting group for diols and carbonyl compounds. It is also used as a starting material for the preparation of silicon-based reagents.
Application
Dichlorodimethylsilane can be used:
- As a silane coupling agent in the synthesis of silica nanoparticles and in their surface modification studies.
- To prepare polydimethylsiloxane microemulsions by reacting with sodium dodecylpolyoxyethylene sulfate.
- To prepare a novel heterasumanene where the benzylic carbon atoms of the sumanene are replaced by heteroatom (S, Si) functionalities
Other Notes
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signalword
Danger
hcodes
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
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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Zhongyan Lu et al.
American journal of physiology. Regulatory, integrative and comparative physiology, 307(5), R558-R570 (2014-06-13)
Ruminal fermentation products such as short-chain fatty acids (SCFA) and CO2 acutely stimulate urea transport across the ruminal epithelium in vivo, whereas ammonia has inhibitory effects. Uptake and signaling pathways remain obscure. The ruminal expression of SLC14a1 (UT-B) was studied
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
Takehiro Fukuzaki et al.
Organic letters, 4(17), 2877-2880 (2002-08-17)
[reaction: see text] Studies on the connection between the right and left segments of azadirachtin are described. The Ireland-Claisen rearrangement of Li-enolate of the modeled ester with dichlorodimethylsilane in toluene afforded the desired limonoid framework stereoselectively in good yield.