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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)-

2,4,6-Trichloroanisole-D5

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Chemical Name: 2,4,6-Trichloroanisole-D5
CAS Number: 352439-08-8
Product Number: AG00BZNW(AGN-PC-0RAOUA)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Properties
MP:
59-61°C
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
216.497g/mol
XLogP3:
4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
214.972g/mol
Monoisotopic Mass:
214.972g/mol
Topological Polar Surface Area:
9.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
119
Isotope Atom Count:
5
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,4,6-Trichloroanisole-d5 is a valuable compound commonly utilized in chemical synthesis for its unique properties. As a deuterated derivative of 2,4,6-Trichloroanisole, it provides significant advantages in various applications. Due to its isotopic labeling with deuterium, it serves as an excellent internal standard in analytical chemistry, allowing for accurate quantification and identification of target compounds in complex mixtures. Additionally, 2,4,6-Trichloroanisole-d5 is frequently employed as a precursor in the synthesis of specialized pharmaceuticals, agrochemicals, and other fine chemicals. Its highly selective incorporation of deuterium atoms enables researchers to study reaction mechanisms, metabolic pathways, and stability profiles with enhanced precision and sensitivity. In essence, 2,4,6-Trichloroanisole-d5 plays a crucial role in advancing the field of chemical synthesis by facilitating the development of novel molecules and enhancing our understanding of chemical processes.