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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)-

Benzene, 1,3,5-tribromo-2-methyl-

Brc1cc(Br)c(c(c1)Br)C Request for Quotation
Chemical Name: Benzene, 1,3,5-tribromo-2-methyl-
CAS Number: 6320-40-7
Product Number: AG003B48(AGN-PC-0JKNFP)
Synonyms:
MDL No:
Molecular Formula: C7H5Br3
Molecular Weight: 328.8266

Identification/Properties

Properties
MP:
68-71 °C(lit.)
BP:
290°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.6340 (estimate)
Computed Properties
Molecular Weight:
328.829g/mol
XLogP3:
4.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
0
Exact Mass:
327.792g/mol
Monoisotopic Mass:
325.794g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
103
Isotope Atom Count:
0
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


1,3,5-Tribromo-2-methylbenzene is a valuable chemical compound extensively utilized in various chemical synthesis processes. Its unique molecular structure allows for versatile applications in organic chemistry. This compound serves as a key building block in the synthesis of pharmaceuticals, agrochemicals, and advanced materials due to its ability to participate in diverse reactions and functionalize specific positions on the benzene ring. In organic synthesis, 1,3,5-Tribromo-2-methylbenzene acts as a halogenated intermediate, enabling the introduction of bromine atoms into organic molecules to create novel structures with desired properties. Its strategic incorporation into complex molecules enhances their chemical reactivity and stability, making it an indispensable reagent for the development of innovative chemical compounds.