1. Home
  2. Acetic acid,2-(4-bromo-2-fluorophenoxy)-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

Acetic acid,2-(4-bromo-2-fluorophenoxy)-

OC(=O)COc1ccc(cc1F)Br Request for Quotation
Chemical Name: Acetic acid,2-(4-bromo-2-fluorophenoxy)-
CAS Number: 451-90-1
Product Number: AG00DQSP(AGN-PC-0RTFM7)
Synonyms:
MDL No:
Molecular Formula: C8H6BrFO3
Molecular Weight: 249.0338

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
249.035g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
247.948g/mol
Monoisotopic Mass:
247.948g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
188
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

Request for Quotation

Customer Feedback

Chemical Structure


2-(4-Bromo-2-fluorophenoxy)acetic acid is a versatile compound commonly utilized in chemical synthesis processes. This compound serves as a valuable building block in the creation of various organic molecules and pharmaceutical intermediates due to its unique structural properties. In chemical synthesis, it functions as a key reagent for the formation of complex organic compounds with specific functionalities. Its bromo and fluoro substituents confer distinct reactivity and allow for precise manipulation of molecular structures during the synthesis of target molecules. Furthermore, the presence of the acetic acid moiety provides a convenient handle for further derivatization, enabling tailored modifications to suit desired chemical properties. The application of 2-(4-Bromo-2-fluorophenoxy)acetic acid in chemical synthesis underscores its significance as a critical component in the development of novel compounds for various industrial and research purposes.