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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)-

Benzeneacetic acid, 2-chloro-4-methoxy-

COc1ccc(c(c1)Cl)CC(=O)O Request for Quotation
Chemical Name: Benzeneacetic acid, 2-chloro-4-methoxy-
CAS Number: 91367-09-8
Product Number: AG006BO0(AGN-PC-0L78T6)
Synonyms:
MDL No:
Molecular Formula: C9H9ClO3
Molecular Weight: 200.6190

Identification/Properties

Properties
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
200.618g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
200.024g/mol
Monoisotopic Mass:
200.024g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
184
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-(2-Chloro-4-methoxyphenyl)acetic acid, also known as $name$, is a valuable compound in chemical synthesis due to its versatile applications. This compound serves as a key intermediate in the production of various pharmaceuticals, agrochemicals, and advanced materials. In organic synthesis, $name$ is commonly used as a building block for the synthesis of complex molecules. It can participate in a range of reactions, including esterifications, amidations, and nucleophilic substitutions, leading to the formation of diverse chemical entities. Additionally, the presence of a chloro and methoxy group in $name$ provides opportunities for further functionalization, enabling the modification of its properties for specific synthetic needs. The unique structural features of 2-(2-Chloro-4-methoxyphenyl)acetic acid make it a crucial component in the development of novel compounds with potential applications across various industries, showcasing its significance in modern chemical synthesis.