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18163-47-8

18163-47-8 | Silane, (2-iodoethynyl)trimethyl-

CAS No: 18163-47-8 Catalog No: AG0022ZB MDL No:MFCD00274201

Product Description

Catalog Number:
AG0022ZB
Chemical Name:
Silane, (2-iodoethynyl)trimethyl-
CAS Number:
18163-47-8
Molecular Formula:
C5H9ISi
Molecular Weight:
224.1149
MDL Number:
MFCD00274201
IUPAC Name:
2-iodoethynyl(trimethyl)silane
InChI:
InChI=1S/C5H9ISi/c1-7(2,3)5-4-6/h1-3H3
InChI Key:
HNIRHTRSZDSMOF-UHFFFAOYSA-N
SMILES:
IC#C[Si](C)(C)C

Properties

Complexity:
109  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
223.952g/mol
Formal Charge:
0
Heavy Atom Count:
7  
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
224.116g/mol
Monoisotopic Mass:
223.952g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
0A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0

Literature

Title Journal
Synthesis and reactivity of an isolable cobalt(I) complex containing a β-diketiminate-based acyclic tetradentate ligand. Inorganic chemistry 20120220
tert-Butyldimethylsilyl O-protected chitosan and chitooligosaccharides: useful precursors for N-modifications in common organic solvents. Carbohydrate research 20081013
Target metabolic profiling analysis of free amino acids in plasma as EOC/TBDMS derivatives by GC-SIM-MS. Biomedical chromatography : BMC 20080401
Regioselective silylation of N-phthaloylchitosan with TBDMS and TBDPS groups. Biomacromolecules 20070601
Unprecedented lability of the 5'-O-tert-butyldimethylsilyl group from 3'-spiro-5''-(4''-acylamino-1'',2''-oxathiole-2'',2''-dioxide) nucleoside derivatives via neighboring group participation of the 4''-acylamino residue. The Journal of organic chemistry 20060217
Determination of thiodiglycol, a mustard gas hydrolysis product by gas chromatography-mass spectrometry after tert-butyldimethylsilylation. Journal of chromatography. A 20041224
New chiral selectors: design and synthesis of 6-TBDMS-2,3-methyl beta-cyclodextrin 2-2' thioureido dimer and 6-TBDMS-2,3-methyl (or 2-methyl-3-acetyl) beta-cyclodextrin bearing an (R) Mosher acid moiety. Chirality 20041001
Discriminative determination of alkyl methylphosphonates and methylphosphonate in blood plasma and urine by gas chromatography-mass spectrometry after tert.-butyldimethylsilylation. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 20030925
Combined isobutoxycarbonylation and tert-butyldimethylsilylation for the GC/MS-SIM detection of alkylphenols, chlorophenols and bisphenol A in mackerel samples. Archives of pharmacal research 20030901
Determination of S-methyl-, S-propyl-, and S-propenyl-L-cysteine sulfoxides by gas chromatography-mass spectrometry after tert-butyldimethylsilylation. Journal of agricultural and food chemistry 20020731
Effect of pedological characteristics on aqueous soil extraction recovery and tert-butyldimethylsilylation yield for gas chromatography-mass spectrometry of nerve gas hydrolysis products from soils. Environmental science & technology 20010501

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