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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)-

4-TERT-BUTYLANILINE-D15

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Chemical Name: 4-TERT-BUTYLANILINE-D15
CAS Number: 1219794-71-4
Product Number: AG009BVM(AGN-009BQ2)
Synonyms:
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Molecular Formula:
Molecular Weight:

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Chemical Structure


4-tert-Butylaniline-d15 is a deuterated derivative of 4-tert-Butylaniline, a versatile compound widely utilized in chemical synthesis. The presence of deuterium in 4-tert-Butylaniline-d15 enhances its chemical stability and provides unique labeling characteristics, making it a valuable tool in various research applications.In chemical synthesis, 4-tert-Butylaniline-d15 serves as a stable isotopically labeled reagent, enabling researchers to trace the molecular pathways of organic reactions with enhanced precision. Its deuterated structure allows for the differentiation of reaction products, intermediates, and side products using analytical techniques such as nuclear magnetic resonance (NMR) spectroscopy.Additionally, the use of 4-tert-Butylaniline-d15 in chemical synthesis facilitates the elucidation of reaction mechanisms, kinetic studies, and isotope labeling experiments. Its selective incorporation into specific functional groups or molecular moieties enables researchers to investigate complex chemical transformations and optimize synthetic routes with a focus on isotope effects.Overall, 4-tert-Butylaniline-d15 offers a valuable resource for chemists and researchers seeking to enhance their understanding of chemical reactions, mechanistic pathways, and molecular dynamics in organic synthesis. Its isotopic labeling properties and chemical stability make it an indispensable component in modern chemical research and development efforts.