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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)-

Benzaldehyde, 3-bromo-5-(trifluoromethyl)-

O=Cc1cc(Br)cc(c1)C(F)(F)F Request for Quotation
Chemical Name: Benzaldehyde, 3-bromo-5-(trifluoromethyl)-
CAS Number: 477535-41-4
Product Number: AG0037TG(AGN-PC-00TXVP)
Synonyms:
MDL No: MFCD08059506
Molecular Formula: C8H4BrF3O
Molecular Weight: 253.0160

Identification/Properties

Computed Properties
Molecular Weight:
253.018g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
251.94g/mol
Monoisotopic Mass:
251.94g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
192
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


3-Bromo-5-(Trifluoromethyl)Benzaldehyde, is a versatile chemical compound widely used in chemical synthesis. It serves as a key building block in the preparation of various functionalized aromatic compounds due to its unique structure and reactivity. This compound is commonly employed as a precursor in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its trifluoromethyl group imparts valuable properties such as increased lipophilicity and electron-withdrawing character, making it particularly useful in drug design and development. In organic chemistry, 3-Bromo-5-(Trifluoromethyl)Benzaldehyde plays a crucial role in the construction of complex molecular structures through various reactions such as nucleophilic substitution, condensation, and aromatic substitution. Its presence in a molecule can also influence its biological activity and pharmacokinetic properties, making it a valuable tool in medicinal chemistry research. Overall, the application of this compound in chemical synthesis allows for the efficient and strategic construction of diverse molecules with specific properties and functions.