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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, (1,1-dimethylethyl)(4-iodobutoxy)dimethyl-

ICCCCO[Si](C(C)(C)C)(C)C Request for Quotation
Chemical Name: Silane, (1,1-dimethylethyl)(4-iodobutoxy)dimethyl-
CAS Number: 92511-12-1
Product Number: AG003ULH(AGN-PC-0L7YOU)
Synonyms:
MDL No:
Molecular Formula: C10H23IOSi
Molecular Weight: 314.2790

Identification/Properties

Properties
BP:
253.1°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Refractive Index:
n20/D 1.48(lit.)
Computed Properties
Molecular Weight:
314.282g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
6
Exact Mass:
314.056g/mol
Monoisotopic Mass:
314.056g/mol
Topological Polar Surface Area:
9.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
140
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:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


tert-Butyl(4-iodobutoxy)dimethylsilane is a highly versatile chemical reagent commonly used in modern organic synthesis. Its unique structure allows for the introduction of both tert-butyl and iodobutoxy functional groups onto a silicon atom, providing a wide range of synthetic possibilities.Due to its bulky tert-butyl group, tert-Butyl(4-iodobutoxy)dimethylsilane is often employed as a sterically hindered nucleophile in various reactions. It can participate in nucleophilic substitution reactions, such as SN2 reactions, with electrophiles to introduce the 4-iodobutoxy moiety into organic molecules. This can be particularly useful in the synthesis of complex organic molecules where precise control over regioselectivity and stereoselectivity is required.Additionally, the dimethylsilane moiety in tert-Butyl(4-iodobutoxy)dimethylsilane can serve as a protecting group for alcohols, amines, or carboxylic acids in organic synthesis. By selectively protecting certain functional groups, chemists can control the reactivity of a molecule and direct reactions to specific sites, enabling the synthesis of intricate molecular structures.In summary, tert-Butyl(4-iodobutoxy)dimethylsilane plays a crucial role in chemical synthesis by serving as a versatile reagent for introducing functional groups and as a protecting group for key functional groups in organic molecules. Its unique structure and reactivity make it an invaluable tool for preparing a diverse array of organic compounds with tailored properties.