Trimethylvinylsilane

Product Information

Molecular Formula:
C5H12Si
Molecular Weight:
100.23
Description
Trimethylvinylsilane is a compound used in the biomedical industry for its potential in developing drugs to treat various diseases. It has shown promise as a key building block in the synthesis of pharmaceutical compounds targeting cancer, neurodegenerative disorders, and infectious diseases. Its unique chemical properties make it an essential component in innovative drug discovery and development processes aimed at improving human health.
Synonyms
Trimethylvinylsilane
IUPAC Name
ethenyl(trimethyl)silane
Canonical SMILES
C[Si](C)(C)C=C
InChI
InChI=1S/C5H12Si/c1-5-6(2,3)4/h5H,1H2,2-4H3
InChI Key
GCSJLQSCSDMKTP-UHFFFAOYSA-N
Boiling Point
55ºC
Melting Point
-132ºC
Flash Point
-24 ℃
Purity
95%
Density
0.684
Appearance
clear colourless liquid
Application
Used in semiconductor processing.
Storage
Flammables area
Refractive Index
n20/D 1.391 (lit.)

Safety Information

Hazards
H225:
Highly flammable liquid and vapour.
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
Precautionary Statement
P210:
Keep away from heat, sparks, open flames, hot surfaces. No smoking.
P233:
Keep container tightly closed.
P264:
Wash thoroughly after handling.
P280:
Wear protective gloves/protective clothing/eye protection/face protection.
P303+P361+P353:
IF ON SKIN (or hair):
Take off immediately all contaminated clothing. [As modified by IV ATP].
Rinse skin with water/shower.
P370+P378:
In case of fire:
Use for extinction:

Computed Properties

Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
1
Exact Mass
100.070826917 g/mol
Monoisotopic Mass
100.070826917 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
6
Formal Charge
0
Complexity
49.4
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114133905-A Organic silicon ceramic tile adhesive and preparation method thereof 2021-12-28
CN-113999395-A Low-alkoxy polysiloxane and preparation method thereof 2021-12-14
CN-114182384-A Method for converting waste mask into regenerated polypropylene fiber 2021-12-14
CN-113956790-A Organic silicon coating and preparation method thereof 2021-12-08
CN-113956776-A Preparation method of powderable self-repairing flame-retardant low-VOC (volatile organic compound) polyurethane coating and application of powderable self-repairing flame-retardant low-VOC polyurethane coating in automobile leather 2021-12-06
CN-114108185-A Preparation method of flame-retardant non-woven fabric and product thereof 2021-12-03
CN-114133487-A Modified cellulose-based polymerization surface agent, emulsification viscosity reducer, preparation method of emulsification viscosity reducer and application of emulsification viscosity reducer in viscosity reduction of thick oil 2021-11-29
CN-113948264-A Iron-nickel magnetic powder core and preparation method thereof 2021-11-18
CN-114163841-A Preparation method and application of polyethylene-coated inorganic particle wear-resistant agent 2021-11-18
CN-114164674-A Aerogel thermal fabric and manufacturing method thereof 2021-11-18

Literatures

PMID Publication Date Title Journal
22834536 2012-08-17 Iron-catalyzed unexpected easy access to stereodefined trimethylsilyl vinyl ketenes Organic letters
21410167 2011-04-15 (E)-9-(2-iodovinyl)-9H-carbazole: a new coupling reagent for the synthesis of π-conjugated carbazoles Organic letters
21114294 2010-12-22 Room-temperature regioselective C-H/olefin coupling of aromatic ketones using an activated ruthenium catalyst with a carbonyl ligand and structural elucidation of key intermediates Journal of the American Chemical Society
20666473 2010-08-25 Development of a general, sequential, ring-closing metathesis/intramolecular cross-coupling reaction for the synthesis of polyunsaturated macrolactones Journal of the American Chemical Society
20198254 2010-03-21 Cobalt-catalyzed regio- and stereoselective intermolecular enyne coupling: an efficient route to 1,3-diene derivatives Chemical communications (Cambridge, England)
19609576 2010-03-01 Quantum chemical studies on substitution effects within silyl group in the silylative coupling of olefins Journal of molecular modeling
19191237 2009-01-01 Palladium-catalyzed cyclopropanation of alkenyl silanes by diazoalkanes: evidence for a Pd(0) mechanism Chemistry (Weinheim an der Bergstrasse, Germany)
18767837 2008-10-01 Why does fluoride anion accelerate transmetalation between vinylsilane and palladium(II)-vinyl complex? Theoretical study Journal of the American Chemical Society
18078507 2007-12-13 Part 3. Triethylborane-air: a suitable initiator for intermolecular radical additions of S-2-oxoalkyl-thionocarbonates (S-xanthates) to olefins Beilstein journal of organic chemistry
17263531 2007-02-21 Scope and mechanism of the intermolecular addition of aromatic aldehydes to olefins catalyzed by Rh(I) olefin complexes Journal of the American Chemical Society
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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