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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)-

4-chloro-2-fluoro-3-methylbenzoic acid

OC(=O)c1ccc(c(c1F)C)Cl Request for Quotation
Chemical Name: 4-chloro-2-fluoro-3-methylbenzoic acid
CAS Number: 153556-55-9
Product Number: AG003L30(AGN-PC-00OUVQ)
Synonyms:
MDL No:
Molecular Formula: C8H6ClFO2
Molecular Weight: 188.5834

Identification/Properties

Properties
BP:
287.1±35.0°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
188.582g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
188.004g/mol
Monoisotopic Mass:
188.004g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
186
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


4-Chloro-2-fluoro-3-methylbenzoic acid, a versatile compound, plays a crucial role in chemical synthesis processes. Its unique molecular structure and properties make it a valuable intermediate in the production of various pharmaceuticals, agrochemicals, and materials. In organic synthesis, this compound serves as a key building block for the creation of more complex chemical structures. Its functional groups allow for diverse reactions, enabling the synthesis of a wide range of compounds with specific characteristics and functions. Additionally, 4-Chloro-2-fluoro-3-methylbenzoic acid can be utilized in the development of new materials with tailored properties, contributing to advancements in various industries. This compound's versatility and reactivity make it a valuable asset in the field of chemical synthesis and pave the way for innovative research and product development.