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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)-

Acetic-1-13C acid, 2,2,2-trichloro-

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Chemical Name: Acetic-1-13C acid, 2,2,2-trichloro-
CAS Number: 173470-69-4
Product Number: AG001YXV(AGN-PC-0QACMR)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Properties
MP:
54-58 °C (lit.)
BP:
196 °C (lit.)

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Trichloroacetic acid-1-^13C is a valuable compound in chemical synthesis, particularly in the field of isotopic labeling. By incorporating a carbon-13 isotope into the trichloroacetic acid structure, it allows for precise tracking and monitoring of chemical reactions in complex systems. This labeled compound serves as a powerful tool in studies ranging from drug metabolism to biomolecular interactions. In organic synthesis, trichloroacetic acid-1-^13C can be utilized as a tracer to investigate reaction mechanisms, identify intermediates, and determine the fate of carbon atoms during transformations. Its unique isotopic signature enables researchers to differentiate between various carbon sources and pathways, offering insights into the formation and transformation of molecules. This compound plays a crucial role in elucidating the intricate processes involved in chemical reactions, ultimately contributing to advancements in organic chemistry and related fields.