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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)-

1,1':4',1''-Terphenyl, 4-bromo-

Brc1ccc(cc1)c1ccc(cc1)c1ccccc1 Request for Quotation
Chemical Name: 1,1':4',1''-Terphenyl, 4-bromo-
CAS Number: 1762-84-1
Product Number: AG0024HN(AGN-PC-0NEF10)
Synonyms:
MDL No:
Molecular Formula: C18H13Br
Molecular Weight: 309.1998

Identification/Properties

Properties
MP:
232 °C
BP:
441.9 °C at 760 mmHg
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
309.206g/mol
XLogP3:
6.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
2
Exact Mass:
308.02g/mol
Monoisotopic Mass:
308.02g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
253
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Bromo-p-terphenyl is a versatile compound widely used in chemical synthesis, particularly in the field of organic chemistry. This compound plays a crucial role in various reactions and processes due to its unique structure and reactivity.One of the key applications of 4-Bromo-p-terphenyl is as a building block in the synthesis of complex organic molecules. Its specific chemical properties allow for the formation of intricate molecular structures that are important in the development of pharmaceuticals, agrochemicals, and advanced materials. By incorporating 4-Bromo-p-terphenyl into a synthesis pathway, chemists can efficiently create diverse compounds with tailored properties for specific applications.Additionally, 4-Bromo-p-terphenyl can act as a precursor in the preparation of functionalized terphenyl derivatives. Through various chemical transformations, this compound can be modified to introduce different functional groups or structural motifs, enabling the synthesis of a wide range of derivatives with diverse properties and applications. This versatility makes 4-Bromo-p-terphenyl a valuable tool in the hands of synthetic chemists striving to design and create novel molecules for various purposes.Overall, the application of 4-Bromo-p-terphenyl in chemical synthesis showcases its significance as a key reagent in organic chemistry, offering opportunities for the creation of complex molecules and tailored compounds with potential use in pharmaceuticals, materials science, and other fields of research and industry.