(Methyl)triphenylphosphonium Iodide-d3,13CD3

Product Name (Methyl)triphenylphosphonium Iodide-d3,13CD3
CAT No. CS-T-58703
CAS No. 282107-30-6
Category Stable Isotopes
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Smileys [2H][13C]([2H])([2H])[P+](C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3.[I-]
Canonical Smiles C[P+](C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3.[I-]
InchIKey JNMIXMFEVJHFNY-SPZGMPHYSA-M
Inchl InChI=1S/C19H18P.HI/c1-20(17-11-5-2-6-12-17,18-13-7-3-8-14-18)19-15-9-4-10-16-19;/h2-16H,1H3;1H/q+1;/p-1/i1+1D3;
IUPAC triphenyl(trideuterio(113C)methyl)phosphanium;iodide
Controlled No
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(Methyl)triphenylphosphonium Iodide-d3,13CD3 is a chemical compound that is commonly used in organic chemistry research and analysis. This compound is a deuterated and isotopically labeled version of the parent compound, (methyl)triphenylphosphonium iodide, which is a white crystalline powder. The deuterated and isotopically labeled version is used to study the behavior and reaction mechanisms of organic compounds in complex chemical systems. One of the main uses of (Methyl)triphenylphosphonium Iodide-d3,13CD3 is as a reagent in organic synthesis. It is commonly used as a catalyst in nucleophilic substitution and elimination reactions, as well as in the synthesis of a variety of organic compounds. The compound is also used as a reference standard in mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy. Chemically, (Methyl)triphenylphosphonium Iodide-d3,13CD3 is composed of a methyl group, three phenyl groups, a phosphonium ion, and an iodide ion. The deuterium and carbon-13 isotopes in the compound allow for the identification and analysis of specific chemical bonds and functional groups in organic molecules. The compound has a molecular weight of 490.38 g/mol and a melting point of approximately 220-222°C. In summary, (Methyl)triphenylphosphonium Iodide-d3,13CD3 is a useful reagent in organic chemistry research and analysis, particularly in the study of complex chemical systems and reaction mechanisms. Its deuterium and carbon-13 isotopes allow for the identification and analysis of specific chemical bonds and functional groups in organic molecules.

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