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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, (chloromethyl)dimethoxymethyl-

ClC[SiH2]C(OC)OC Request for Quotation
Chemical Name: Silane, (chloromethyl)dimethoxymethyl-
CAS Number: 2212-11-5
Product Number: AG00I4CI(AGN-PC-0BT69Z)
Synonyms:
MDL No:
Molecular Formula: C4H11ClO2Si
Molecular Weight: 154.66744

Identification/Properties

Computed Properties
Molecular Weight:
154.665g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
154.022g/mol
Monoisotopic Mass:
154.022g/mol
Topological Polar Surface Area:
18.5A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
65.1
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:
H226-H319
Precautionary Statements:
P305+P351+P338
Class:
3
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


(Chloromethyl)dimethoxy(methyl)silane is a versatile reagent widely used in chemical synthesis for its unique properties and ability to react with a variety of functional groups. This compound serves as an important building block in organic synthesis, particularly in the preparation of organosilicon compounds.In chemical synthesis, (Chloromethyl)dimethoxy(methyl)silane can be utilized as a silylating agent to introduce silicon-containing functionalities into organic molecules. It is commonly employed in the protection of sensitive functional groups during multi-step reactions, as well as in the modification of polymers to impart new properties. Additionally, this compound can participate in nucleophilic substitution reactions, leading to the formation of new carbon-silicon bonds.Furthermore, (Chloromethyl)dimethoxy(methyl)silane finds application in the synthesis of organosilicon compounds with diverse applications, including in materials science, pharmaceuticals, and agrochemicals. Its reactivity and compatibility with a wide range of substrates make it a valuable tool for organic chemists seeking to functionalize molecules with silicon-containing moieties.