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Merck

440272

Sigma-Aldrich

二氯二甲基硅烷

≥99.5%

别名:

DMDCS, 二甲基二氯硅烷

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About This Item

线性分子式:
(CH3)2SiCl2
CAS号:
分子量:
129.06
Beilstein:
605287
EC號碼:
MDL號碼:
分類程式碼代碼:
12352103
PubChem物質ID:
NACRES:
NA.22

化驗

≥99.5%

形狀

liquid

折射率

n20/D 1.404 (lit.)

bp

70 °C (lit.)

mp

−76 °C (lit.)

密度

1.07 g/mL at 25 °C (lit.)

儲存溫度

2-8°C

SMILES 字串

C[Si](C)(Cl)Cl

InChI

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

InChI 密鑰

LIKFHECYJZWXFJ-UHFFFAOYSA-N

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應用

用于与叔醇反应制备树脂键合硅氧烷。
用于合成光学活性柄型金属茂聚合催化剂的常用试剂。

訊號詞

Danger

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

33.8 °F - closed cup

閃點(°C)

1 °C - closed cup

個人防護裝備

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


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Tetrahedron, 63, 299-299 (2007)
Raimundo Ho et al.
International journal of pharmaceutics, 387(1-2), 79-86 (2009-12-17)
The sensitivity of two techniques in tracking changes in surface energetics was investigated for a crystalline excipient, D-mannitol. Macroscopic crystals of D-mannitol were grown from saturated water solution by slow cooling, and sessile drop contact angle was employed to measure
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
S N Krylov et al.
Electrophoresis, 21(4), 767-773 (2000-03-25)
Capillary electrophoresis (CE) is an important tool of chemical cytometry. Whole-cell analysis using CE starts with cell injection into the capillary by either siphoning or electroosmosis. However, strong adherence of the cell to the support surface can prevent efficient cell
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.

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