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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, chloro(3-chloropropyl)dimethyl-

ClCCC[Si](Cl)(C)C Request for Quotation
Chemical Name: Silane, chloro(3-chloropropyl)dimethyl-
CAS Number: 10605-40-0
Product Number: AG008S4C(AGN-PC-0JLU3P)
Synonyms:
MDL No:
Molecular Formula: C5H12Cl2Si
Molecular Weight: 171.14028

Identification/Properties

Computed Properties
Molecular Weight:
171.136g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
3
Exact Mass:
170.009g/mol
Monoisotopic Mass:
170.009g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
63.4
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

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(Chlorodimethylsilyl)propyl chloride is a versatile chemical reagent commonly used in chemical synthesis processes. This compound is valued for its ability to introduce functional groups such as silyl chlorides into organic molecules, making it a valuable tool in the field of organic chemistry. In particular, 3-(Chlorodimethylsilyl)propyl chloride is frequently employed as a reagent for the protection of hydroxyl groups in various organic compounds. By reacting with hydroxyl groups, this compound can effectively block their reactivity, allowing for selective functionalization of other parts of the molecule. Additionally, 3-(Chlorodimethylsilyl)propyl chloride can also serve as a precursor for the synthesis of silyl ethers, which are commonly used as protecting groups in organic synthesis to prevent unwanted reactions or to control regioselectivity. Furthermore, this reagent can participate in various coupling reactions to form carbon-silicon bonds, expanding its utility in the synthesis of complex organic molecules. Overall, the unique properties of 3-(Chlorodimethylsilyl)propyl chloride make it a valuable reagent for manipulating and modifying organic compounds in chemical synthesis processes.