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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, 4-(bromomethyl)-1-chloro-2-(trifluoromethyl)-

BrCc1ccc(c(c1)C(F)(F)F)Cl Request for Quotation
Chemical Name: Benzene, 4-(bromomethyl)-1-chloro-2-(trifluoromethyl)-
CAS Number: 261763-23-9
Product Number: AG002S2Q(AGN-PC-0KKYOB)
Synonyms:
MDL No:
Molecular Formula: C8H5BrClF3
Molecular Weight: 273.4775

Identification/Properties

Properties
MP:
36-40℃
BP:
233.9°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
273.477g/mol
XLogP3:
4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
271.922g/mol
Monoisotopic Mass:
271.922g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
171
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:
Danger
UN#:
1759
Hazard Statements:
H314-H318
Precautionary Statements:
P260-P280-P305+P351+P338-P309-P310
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Chloro-3-trifluoromethylbenzyl bromide, also known as $name$, serves as a versatile building block in organic synthesis. This compound plays a crucial role in the construction of complex organic molecules by facilitating key reactions and functional group modifications. With its unique structural attributes, 4-Chloro-3-trifluoromethylbenzyl bromide is widely employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its ability to react selectively with various nucleophiles, such as amines, alcohols, and thiols, makes it a valuable reagent in the preparation of diverse chemical entities. Additionally, the incorporation of the trifluoromethyl group enhances the physicochemical properties of the final products, leading to improved bioactivity and stability. Embraced by synthetic chemists, 4-Chloro-3-trifluoromethylbenzyl bromide continues to fuel innovation and discovery in the field of organic chemistry.