1. Home
  2. Silane, ethyldimethyl-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Silane, ethyldimethyl-

CC[SiH](C)C Request for Quotation
Chemical Name: Silane, ethyldimethyl-
CAS Number: 758-21-4
Product Number: AG008P88(AGN-PC-0JL99N)
Synonyms:
MDL No:
Molecular Formula: C4H12Si
Molecular Weight: 88.2236

Identification/Properties

Computed Properties
Molecular Weight:
87.217g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
1
Exact Mass:
87.063g/mol
Monoisotopic Mass:
87.063g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
5
Formal Charge:
0
Complexity:
17.6
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

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
1993
Hazard Statements:
H225-H315-H319-H335
Precautionary Statements:
P210-P233-P235-P240-P241-P242-P243-P260-P261-P264-P271-P280-P302+P352-P303+P361+P353-P304-P304+P340-P305+P351+P338-P312-P321-P332+P313-P337+P313-P340-P362-P370+P378-P403-P403+P233-P403+P235-P405-P501
Class:
3
Packing Group:
Ⅱ

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Ethyldimethylsilane, also known as trimethyl(vinyl)silane, plays a crucial role in chemical synthesis as a versatile building block in organic reactions. This organosilicon compound is utilized primarily as a reagent in various transformations to introduce functional groups into organic molecules. In the presence of suitable catalysts or under specific reaction conditions, ethyldimethylsilane can participate in hydrosilylation reactions, where the silicon-carbon bond is formed via the addition of a silicon hydride group across a carbon-carbon double bond. This reaction is widely employed in the synthesis of silicon-containing polymers, as well as in the functionalization of organic molecules to modify their properties. Additionally, ethyldimethylsilane serves as a precursor for the introduction of silicon-based functionalities in organic compounds, allowing for the creation of novel materials with unique properties and applications in various fields of chemistry and materials science.