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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, 1,2,4-tribromo-

Brc1ccc(c(c1)Br)Br Request for Quotation
Chemical Name: Benzene, 1,2,4-tribromo-
CAS Number: 615-54-3
Product Number: AG003DB6(AGN-PC-0JKACW)
Synonyms:
MDL No:
Molecular Formula: C6H3Br3
Molecular Weight: 314.8000

Identification/Properties

Properties
MP:
41-43 °C(lit. )
BP:
277.3°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
>110^o(230^oF)
Computed Properties
Molecular Weight:
314.802g/mol
XLogP3:
4.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
0
Exact Mass:
313.776g/mol
Monoisotopic Mass:
311.778g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
94.3
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,2,4-Tribromobenzene is a versatile chemical compound that finds wide application in chemical synthesis. As a substituted benzene derivative, it serves as a key building block in the creation of various organic compounds. In particular, 1,2,4-Tribromobenzene is commonly used in the synthesis of pharmaceuticals, agrochemicals, and materials science.Its bromine atoms provide a unique reactivity, allowing for selective functionalization at specific positions on the benzene ring. This enables chemists to control the structure and properties of the resulting molecules with precision. Additionally, the presence of three bromine substituents imparts distinct chemical and physical properties, making 1,2,4-Tribromobenzene a valuable intermediate in the development of novel compounds.In organic synthesis, 1,2,4-Tribromobenzene can undergo various reactions such as substitution, reduction, and coupling reactions to create complex molecules with specific functionalities. Its versatility and reactivity make it an indispensable tool for synthetic chemists seeking to design and produce new compounds for a range of applications.