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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)-

3-Chloro-2-fluorocinnamic acid

OC(=O)C=Cc1cccc(c1F)Cl Request for Quotation
Chemical Name: 3-Chloro-2-fluorocinnamic acid
CAS Number: 261762-62-3
Product Number: AG002S11(AGN-PC-0KKVKX)
Synonyms:
MDL No:
Molecular Formula: C9H6ClFO2
Molecular Weight: 200.5941

Identification/Properties

Properties
BP:
326.1°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
200.593g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
200.004g/mol
Monoisotopic Mass:
200.004g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
218
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
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


The 3-(3-chloro-2-fluorophenyl)acrylic acid is a versatile compound widely used in chemical synthesis. Its unique chemical properties make it a valuable building block for the creation of various organic compounds. In organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and materials with specific functionalities. Its ability to undergo multiple chemical reactions, such as nucleophilic addition and substitution reactions, enables the creation of complex molecular structures. Additionally, the presence of both a chloro and fluoro group on the phenyl ring provides opportunities for further modification and diversification of the compound, resulting in a wide array of potential applications in the field of organic chemistry.