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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, chloro-2-hydroxy-

OC(=O)c1cccc(c1O)Cl Request for Quotation
Chemical Name: Benzoic acid, chloro-2-hydroxy-
CAS Number: 1829-32-9
Product Number: AG002488(AGN-PC-0JLBPL)
Synonyms:
MDL No:
Molecular Formula: C7H5ClO3
Molecular Weight: 172.5658

Identification/Properties

Computed Properties
Molecular Weight:
172.564g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
171.993g/mol
Monoisotopic Mass:
171.993g/mol
Topological Polar Surface Area:
57.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
160
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


3-Chloro-2-hydroxybenzoic acid, also known as Salicyloyl chloride, is a versatile compound commonly used in chemical synthesis processes. With its unique structure and properties, 3-Chloro-2-hydroxybenzoic acid is frequently employed as a key intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals.One of the primary applications of 3-Chloro-2-hydroxybenzoic acid in chemical synthesis is its role as a crucial building block in the synthesis of salicylate derivatives. By selectively reacting with other functional groups under controlled conditions, this compound allows for the efficient modification and derivatization of salicylic acid-based molecules, leading to the creation of new pharmaceutical compounds with improved properties and enhanced biological activities.Furthermore, 3-Chloro-2-hydroxybenzoic acid serves as a valuable reagent in the preparation of esters, amides, and other organic compounds through various synthetic routes. Its reactivity and ability to undergo selective chemical transformations make it an essential component in the development of novel materials and substances with diverse applications in the chemical industry.Overall, the versatile nature of 3-Chloro-2-hydroxybenzoic acid makes it a key player in chemical synthesis, enabling the synthesis of complex molecules and facilitating the discovery of innovative compounds with significant commercial and scientific implications.