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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, 2,4-dibromo-6-fluoro-

O=Cc1c(F)cc(cc1Br)Br Request for Quotation
Chemical Name: Benzaldehyde, 2,4-dibromo-6-fluoro-
CAS Number: 205683-34-7
Product Number: AG002A9P(AGN-PC-0KKVTK)
Synonyms:
MDL No:
Molecular Formula: C7H3Br2FO
Molecular Weight: 281.9045

Identification/Properties

Computed Properties
Molecular Weight:
281.906g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
281.851g/mol
Monoisotopic Mass:
279.853g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
153
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


2,4-Dibromo-6-fluorobenzaldehyde is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. Its applications in organic chemistry are diverse, making it an essential reagent in various reactions.In organic synthesis, 2,4-Dibromo-6-fluorobenzaldehyde is commonly employed as a building block for the assembly of complex molecules. Its electrophilic nature allows it to participate in diverse reactions such as nucleophilic substitution, condensation, and cyclization reactions. One of the key applications of 2,4-Dibromo-6-fluorobenzaldehyde is in the synthesis of biologically active compounds. By incorporating this compound into the molecular structure, chemists can modulate the properties of the final product, leading to potential drug candidates or new materials with specific functions.Furthermore, 2,4-Dibromo-6-fluorobenzaldehyde can also serve as a precursor for various heterocyclic compounds and organic dyes. Its ability to undergo multiple transformations under different reaction conditions makes it a valuable tool for the creation of complex organic molecules with diverse applications.Overall, the versatility and reactivity of 2,4-Dibromo-6-fluorobenzaldehyde make it a valuable asset in the arsenal of synthetic chemists, enabling the efficient and precise construction of intricate chemical structures for a wide range of applications in the field of organic chemistry.