1. Home
  2. Benzoic acid, 3,5-dichloro-2-hydroxy-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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, 3,5-dichloro-2-hydroxy-

Clc1cc(Cl)c(c(c1)C(=O)O)O Request for Quotation
Chemical Name: Benzoic acid, 3,5-dichloro-2-hydroxy-
CAS Number: 320-72-9
Product Number: AG003ILG(AGN-PC-0JK91Q)
Synonyms:
MDL No:
Molecular Formula: C7H4Cl2O3
Molecular Weight: 207.0109

Identification/Properties

Properties
MP:
221-224 °C
BP:
319.3°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Refractive Index:
1.4845 (estimate)
Solubility:
Solubility in methanol (almost transparency).
Computed Properties
Molecular Weight:
207.006g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
205.954g/mol
Monoisotopic Mass:
205.954g/mol
Topological Polar Surface Area:
57.5A^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

Request for Quotation

Customer Feedback

Chemical Structure


3,5-Dichloro-2-hydroxybenzoic acid, also known as dichlorosalicylic acid, is a versatile compound commonly employed in chemical synthesis. This compound serves various essential roles in the field of chemistry, particularly in organic synthesis and pharmaceutical research.One prominent application of 3,5-Dichloro-2-hydroxybenzoic acid is its utility as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its unique molecular structure provides a valuable building block for the creation of diverse organic compounds with specific properties and functions. By incorporating this compound into reaction pathways, chemists can access a wide range of structurally intricate molecules that may exhibit biological activity or desirable chemical properties.Furthermore, 3,5-Dichloro-2-hydroxybenzoic acid is often utilized as a precursor for the synthesis of specialized chemical reagents. Through appropriate derivatization or functional group modifications, this compound can be transformed into derivatives with tailored reactivity or selectivity. These modified derivatives play crucial roles in various chemical transformations, enabling the efficient synthesis of complex molecules and facilitating the development of novel materials.In addition to its direct involvement in chemical reactions, 3,5-Dichloro-2-hydroxybenzoic acid also appears in the formulation of certain dyes and pigments. Its structural characteristics contribute to the vibrancy and stability of the resulting colored compounds, making it a valuable component in the production of high-quality colorants for industrial and commercial applications.Overall, 3,5-Dichloro-2-hydroxybenzoic acid's significance in chemical synthesis lies in its versatility and adaptability across different areas of research and development. Through strategic utilization of this compound, chemists can unlock new possibilities in organic chemistry, pharmaceutical discovery, and materials science.