26253
(3-Chloropropyl)trimethylsilane
≥97.0%
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About This Item
Empirical Formula (Hill Notation):
C6H15ClSi
CAS Number:
Molecular Weight:
150.72
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
219-059-0
Beilstein/REAXYS Number:
1732625
MDL number:
Assay:
≥97.0%
InChI key
QXDDDCNYAAJLBT-UHFFFAOYSA-N
InChI
1S/C6H15ClSi/c1-8(2,3)6-4-5-7/h4-6H2,1-3H3
SMILES string
C[Si](C)(C)CCCCl
assay
≥97.0%
refractive index
n20/D 1.431
bp
151 °C (lit.)
density
0.878 g/mL at 20 °C (lit.)
functional group
chloro
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
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
120.2 °F - closed cup
flash_point_c
49 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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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)
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)
New deoxynojirimycin derivatives as potent inhibitors of intestinal a-glucohydrolases.
Lesur B, et al.
Bioorganic & Medicinal Chemistry Letters, 7(3), 355-360 (1997)
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