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Chlorotrimethylsilane

An organic compound, C3H9ClSi, 108.644 g/mol. Boiling point 57 °C, melting point -40 °C, as published.

verified record, Organic compound, 7 measured properties

Identifiers

Molecular formula
C₃H₉ClSi
Molecular weight
108.644 g/mol
Exact mass
108.016204 g/mol
SMILES
C[Si](C)(C)Cl
InChI
InChI=1S/C3H9ClSi/c1-5(2,3)4/h1-3H3
InChIKey
IJOOHPMOJXWVHK-UHFFFAOYSA-N

Measured properties

Published measurements, each with its source. Two readings of one property are both shown, in the units each used.

Boiling Point
135 °F at 760 mmHg (EPA, 1998)measured · U.S. Environmental Protection Agency. 1998. Extremely Hazardous Substances (EHS) Chemical Profiles and Emergency First Aid Guides. Washington, D.C.: U.S. Government Printing Office.
57 °Cmeasured · Lewis, R.J. Sr.; Hawley's Condensed Chemical Dictionary 14th Edition. John Wiley & Sons, Inc. New York, NY 2001., p. 1132
57 °Cmeasured · reference compound database
57 °C @760 [mm Hg]measured · reference compound database
Melting Point
-72 °F (EPA, 1998)measured · U.S. Environmental Protection Agency. 1998. Extremely Hazardous Substances (EHS) Chemical Profiles and Emergency First Aid Guides. Washington, D.C.: U.S. Government Printing Office.
-40 °Cmeasured · Lewis, R.J. Sax's Dangerous Properties of Industrial Materials. 10th ed. Volumes 1-3 New York, NY: John Wiley & Sons Inc., 1999., p. V3: 3586
-58 °Cmeasured · reference compound database
-40 °Cmeasured · reference compound database
Flash Point
0 °F (EPA, 1998)measured · U.S. Environmental Protection Agency. 1998. Extremely Hazardous Substances (EHS) Chemical Profiles and Emergency First Aid Guides. Washington, D.C.: U.S. Government Printing Office.
[ERG 2016] -28 °Cmeasured · reference compound database
-18 °F (-28 °C) (Closed cup)measured · Fire Protection Guide to Hazardous Materials. 13 ed. Quincy, MA: National Fire Protection Association, 2002., p. 325-111
0 °F (Open cup)measured · U.S. Coast Guard, Department of Transportation. CHRIS - Hazardous Chemical Data. Volume II. Washington, D.C.: U.S. Government Printing Office, 1984-5.
-27 °Cmeasured · reference compound database
Solubility
Decomposes (NTP, 1992)measured · National Toxicology Program, Institute of Environmental Health Sciences, National Institutes of Health (NTP). 1992. National Toxicology Program Chemical Repository Database. Research Triangle Park, North Carolina.
Sol in benzene, ether, perchloroethylenemeasured · Lewis, R.J. Sr.; Hawley's Condensed Chemical Dictionary 14th Edition. John Wiley & Sons, Inc. New York, NY 2001., p. 1132
Solubility in water: reactionmeasured · reference compound database
Density
0.854 at 77 °F (EPA, 1998) - Less dense than water; will floatmeasured · U.S. Environmental Protection Agency. 1998. Extremely Hazardous Substances (EHS) Chemical Profiles and Emergency First Aid Guides. Washington, D.C.: U.S. Government Printing Office.
0.854 AT 25 °C/25 °Cmeasured · Lewis, R.J. Sr.; Hawley's Condensed Chemical Dictionary 14th Edition. John Wiley & Sons, Inc. New York, NY 2001., p. 1132
Relative density (water = 1): 0.85measured · reference compound database
0.854 @25 °Cmeasured · reference compound database
Vapor Pressure
608 mmHg at 68 °F ; 40 mmHg at 11.5 °F; 100 mmHg at 42.8 °F (NTP, 1992)measured · National Toxicology Program, Institute of Environmental Health Sciences, National Institutes of Health (NTP). 1992. National Toxicology Program Chemical Repository Database. Research Triangle Park, North Carolina.
234.0 [mmHg]measured · reference compound database
234 mm Hg at 25 °Cmeasured · Boublik, T., Fried, V., and Hala, E., The Vapour Pressures of Pure Substances. Second Revised Edition. Amsterdam: Elsevier, 1984., p. 42
Vapor pressure, kPa at 20 °C: 26.7measured · reference compound database
Refractive Index
Index of refraction = 1.3870 at 25 °C/Dmeasured · Lide, D.R., G.W.A. Milne (eds.). Handbook of Data on Organic Compounds. Volume I. 3rd ed. CRC Press, Inc. Boca Raton ,FL. 1994., p. V5: 4927

Calculated properties

Derived from the structure, not from a sample; kept apart from the measurements above.

logP
2.0601calculated · chemistry engine
Estimated preference for oil over water. Higher means more oil-like.
Topological polar surface area
0 Ųcalculated · chemistry engine
Surface area from polar atoms; relates to how easily a molecule crosses membranes.
H-bond donors
0calculated · chemistry engine
Atoms that can donate a hydrogen bond.
H-bond acceptors
0calculated · chemistry engine
Atoms that can accept a hydrogen bond.
Rotatable bonds
0calculated · chemistry engine
Single bonds the molecule can freely twist around.
Molar refractivity
29.199 cm³/molcalculated · chemistry engine
Relates to the molecule's polarisability.
Fraction sp³ carbons
1calculated · chemistry engine
Share of carbon atoms with tetrahedral bonding.
QED drug-likeness
0.3293calculated · chemistry engine
Quantitative estimate of drug-likeness (0–1).

What it is made of

Elements

Percentages are of the molecular weight above, worked out the same way the molar mass calculator does it.

Structure

Heavy atoms, hydrogen excluded
5
Total atoms, hydrogen included
14
Rings
0
Aromatic rings
0
Stereocentres
0
Formal charge
0

The molecule in three dimensions

Rotate and inspect the atoms. Loaded only when you ask, so the page stays light.

The drawing above is a diagram of what is bonded to what. A molecule is not flat, and the model here is one low-energy shape generated from the connectivity — useful for seeing which groups can reach each other, and not a measured structure. A real sample is a population of conformations, interconverting.

Reactions it appears in

No documented reaction with a written procedure and a source involves Chlorotrimethylsilane yet.

Other names for it

No systematic name is recorded.

The sources also call it TRIMETHYLCHLOROSILANE, Trimethylsilyl chloride, Silane, chlorotrimethyl-, Trimethyl chlorosilane, Monochlorotrimethylsilicon, Silane, trimethylchloro-, Silicane, chlorotrimethyl-, Silylium, trimethyl-, chloride, trimethylsilane chloride, monochlorotrimethylsilane, trimethyl silyl chloride, Chlorotrimethylsilicane.

Structurally related

Nothing structurally close to Chlorotrimethylsilane has a page here yet.

Seen alongside it in reaction records

Molecules that appear in the same recorded reactions as Chlorotrimethylsilane. This says nothing about structure: most of them are the bases, solvents, ligands and catalysts the chemistry needed, and they are here because somebody put them in the same flask.

Where these values came from

  • chemistry engine

    structure perception

compound record.

What this page does not claim

Identifiers are copied from the source record, measured values are reported as published, and calculated values are marked as calculated. Nothing here is a hazard, purity or handling assessment — how the library is checked.