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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)-

2-Bromo-6-fluorobenzoyl chloride

ClC(=O)c1c(F)cccc1Br Request for Quotation
Chemical Name: 2-Bromo-6-fluorobenzoyl chloride
CAS Number: 1020718-20-0
Product Number: AG0006J7(AGN-PC-056MYF)
Synonyms:
MDL No:
Molecular Formula: C7H3BrClFO
Molecular Weight: 237.4535

Identification/Properties

Computed Properties
Molecular Weight:
237.452g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
235.904g/mol
Monoisotopic Mass:
235.904g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
165
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#:
3265
Hazard Statements:
H314-H318
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Bromo-6-fluorobenzoyl chloride is a versatile compound commonly used in chemical synthesis as a key building block for the creation of various pharmaceuticals, agrochemicals, and materials. Its unique chemical properties make it a valuable reagent in organic chemistry, particularly in the formation of complex molecules through acylation reactions. By serving as an acylating agent, 2-Bromo-6-fluorobenzoyl chloride can facilitate the introduction of the benzoyl group into a wide range of organic molecules, enabling the synthesis of compounds with desired medicinal or chemical properties. This compound plays a crucial role in the development of innovative molecules and materials with diverse applications in industry and research.