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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)-

Phen-2,3,5,6-d4-ol, 4-bromo-

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Chemical Name: Phen-2,3,5,6-d4-ol, 4-bromo-
CAS Number: 152404-44-9
Product Number: AG00AB13(AGN-PC-0Q6BDQ)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
177.033g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
175.977g/mol
Monoisotopic Mass:
175.977g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
66.9
Isotope Atom Count:
4
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


4-Bromophenol-2,3,5,6-d4, a deuterated derivative of 4-bromophenol, serves as a valuable precursor in chemical synthesis for isotopic labeling applications. Its unique isotopic composition, with deuterium atoms replacing the hydrogen atoms in specific positions, allows for accurate tracking and elucidation of reaction pathways in complex chemical transformations. This isotopically substituted compound finds use in a diverse range of research areas, including organic synthesis, medicinal chemistry, and biochemical studies, where precise manipulation of isotopic labeling is crucial for understanding molecular mechanisms. By incorporating 4-Bromophenol-2,3,5,6-d4 into synthetic pathways, researchers can gain critical insights into reaction mechanisms, metabolic pathways, and molecular interactions, pushing the boundaries of scientific discovery in the field of chemistry.