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About This Item
Empirical Formula (Hill Notation):
C6H15ClSi
CAS Number:
Molecular Weight:
150.72
Beilstein:
1732625
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
≥97.0%
refractive index
n20/D 1.431
bp
151 °C (lit.)
density
0.878 g/mL at 20 °C (lit.)
SMILES string
C[Si](C)(C)CCCCl
InChI
1S/C6H15ClSi/c1-8(2,3)6-4-5-7/h4-6H2,1-3H3
InChI key
QXDDDCNYAAJLBT-UHFFFAOYSA-N
Application
(3-Chloropropyl)trimethylsilane has been used in the preparation of:
- 8-(3-trimethylsilylpropoxy)quinolone under phase transfer catalytic conditions
- 5-trimethylsilyl pentanol
- N-(tri-methylsilylalkyl)diamines
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
120.2 °F - closed cup
Flash Point(C)
49 °C - closed cup
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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Find documentation for the products that you have recently purchased in the Document Library.
New deoxynojirimycin derivatives as potent inhibitors of intestinal a-glucohydrolases.
Lesur B, et al.
Bioorganic & Medicinal Chemistry Letters, 7(3), 355-360 (1997)
Organosilicon Compounds. Part V. Synthesis of N-(trimethylsilylalkyl) diamines and N-(trimethylsilylalkyl)-N'-(2-mercaptoethyl) diamines.
Thames SF and Edwards LH.
J. Chem. Soc. Sect. C, 2339-2342 (1968)
Silyl Modification of Biologically Active Compounds. 10. Lipid Type Organosilicon Derivatives of 8-Hydroxyquinoline and N-(2-Hydroxyethyl)-1, 2, 3, 4-tetrahydro (sila, iso) quinolines.
Segal I, et al.
Chemistry of Heterocyclic Compounds, 41(5), 613-624 (2005)
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