Home Other Building Blocks trimethyliodosilane

trimethyliodosilane

CAS No.:
16029-98-4
Catalog Number:
AG0035UM
Molecular Formula:
C3H9ISi
Molecular Weight:
200.0935
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
95%
In Stock USA
United States
$57
- +
100g
95%
In Stock USA
United States
$478
- +
Product Description
Catalog Number:
AG0035UM
Chemical Name:
trimethyliodosilane
CAS Number:
16029-98-4
Molecular Formula:
C3H9ISi
Molecular Weight:
200.0935
MDL Number:
MFCD00001028
IUPAC Name:
iodo(trimethyl)silane
InChI:
InChI=1S/C3H9ISi/c1-5(2,3)4/h1-3H3
InChI Key:
CSRZQMIRAZTJOY-UHFFFAOYSA-N
SMILES:
C[Si](I)(C)C
EC Number:
240-171-0
Properties
Complexity:
28.4  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
199.952g/mol
Formal Charge:
0
Heavy Atom Count:
5  
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
200.094g/mol
Monoisotopic Mass:
199.952g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
0A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Literature
Title Journal
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Environmentally responsive 'hairy' nanoparticles: mixed homopolymer brushes on silica nanoparticles synthesized by living radical polymerization techniques. Journal of the American Chemical Society 20050504
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Synthesis, characterization and coordination chemistry of a macrocyclic ligand containing arsenic donors. Dalton transactions (Cambridge, England : 2003) 20050207
MgI2-catalyzed halo aldol reaction: a practical approach to (E)-beta-iodovinyl-beta'-hydroxyketones. Organic & biomolecular chemistry 20041021
Application of a simple and sensitive GC-MS method for determination of morphine in the hair of opium abusers. Analytical and bioanalytical chemistry 20040501
Unique reactions of glycosyl iodides with oxa- and thiocycloalkane acceptors. Organic letters 20040318
Auto-ionization in lutetium iodide complexes: effect of the Iioic radius on lanthanide-iodide binding. Inorganic chemistry 20040209
N-methyl-N-trimethylsilyltrifluoroacetamide-promoted synthesis and mass spectrometric characterization of deuterated ephedrines. European journal of mass spectrometry (Chichester, England) 20040101
Efficient route to 2-deoxy beta-O-aryl-d-glycosides via direct displacement of glycosyl iodides. Organic letters 20031030
The remarkable ability of lithium ion to reverse the stereoselectivity in the conjugate addition of Li[BuCuI] to a chiral N-crotonyl-2-oxazolidinone. Organic letters 20030918
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An expeditious and efficient procedure for the synthesis of unsaturated acyclonucleosides of Z configuration related to D4T. The Journal of organic chemistry 20030207
Facile and stereoselective access to nonracemic tricyclic cyclobutanes by asymmetric intramolecular Michael-aldol reaction: thermodynamic equilibrium and activation by iodonium ion. The Journal of organic chemistry 20010629
Reductive cleavage of heteroaryl c-halogen bonds by iodotrimethylsilane. Facile and regioselective dechlorination of antibiotic pyrrolnitrin. The Journal of organic chemistry 20010518
Reduction of acetals with samarium diiodide in acetonitrile in the presence of Lewis acids. Chemical & pharmaceutical bulletin 20010101
Properties