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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, chlorotripropyl-

CCC[Si](CCC)(CCC)Cl Request for Quotation
Chemical Name: Silane, chlorotripropyl-
CAS Number: 995-25-5
Product Number: AG003OUP(AGN-PC-0JL9P8)
Synonyms:
MDL No:
Molecular Formula: C9H21ClSi
Molecular Weight: 192.8015

Identification/Properties

Properties
Storage:
Room Temperature;Inert atmosphere;
Computed Properties
Molecular Weight:
192.802g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
6
Exact Mass:
192.11g/mol
Monoisotopic Mass:
192.11g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
76.5
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Chlorotrimethylsilane is a versatile organosilicon compound commonly used in chemical synthesis as a key reagent for various reactions, thanks to its unique properties. As a silylating agent, it is frequently employed for the protection of alcohols, amines, and carboxylic acids in organic synthesis. Additionally, it serves as a precursor for the introduction of trimethylsilyl (TMS) groups in organic molecules, enabling easier manipulation and analysis by techniques such as mass spectrometry and NMR spectroscopy. Furthermore, Chlorotrimethylsilane is utilized in the preparation of functionalized silanes, which find application in materials science for surface modification, adhesion promotion, and as coupling agents in the synthesis of hybrid organic-inorganic materials. Its ability to selectively react with hydroxyl groups makes it a valuable tool in the modification of polymers, resins, and other organic compounds, enhancing their performance properties.