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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)-

Benzoic acid, 2-chloro-6-methoxy-

COc1cccc(c1C(=O)O)Cl Request for Quotation
Chemical Name: Benzoic acid, 2-chloro-6-methoxy-
CAS Number: 3260-89-7
Product Number: AG00C6Z3(AGN-PC-0JLQ8O)
Synonyms:
MDL No:
Molecular Formula: C8H7ClO3
Molecular Weight: 186.5924

Identification/Properties

Computed Properties
Molecular Weight:
186.591g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
186.008g/mol
Monoisotopic Mass:
186.008g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
172
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


2-Chloro-6-methoxybenzoic acid, also known as O-Anisic acid, serves a crucial role in chemical synthesis as a versatile building block. This compound acts as a key intermediate in the preparation of various compounds, particularly in the pharmaceutical and agrochemical industries. Its unique chemical structure allows for functional group manipulation, enabling the synthesis of diverse molecules with desired properties.In chemical synthesis, 2-Chloro-6-methoxybenzoic acid can undergo various reactions such as esterification, halogenation, and coupling reactions to introduce different functional groups. These reactions lead to the formation of novel compounds used in drug discovery, material science, and pesticide development. Additionally, the presence of both a chlorine atom and a methoxy group provides opportunities for regioselective and stereoselective transformations, making this compound valuable in complex molecule synthesis.Overall, 2-Chloro-6-methoxybenzoic acid is a crucial reagent in chemical synthesis, offering synthetic chemists the flexibility to design and access a wide range of molecular structures for various applications.