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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, 2,3,5-trichloro-

Clc1cc(Cl)c(c(c1)C(=O)O)Cl Request for Quotation
Chemical Name: Benzoic acid, 2,3,5-trichloro-
CAS Number: 50-73-7
Product Number: AG003FF5(AGN-PC-0JL6ZW)
Synonyms:
MDL No:
Molecular Formula: C7H3Cl3O2
Molecular Weight: 225.4565

Identification/Properties

Properties
MP:
163-168 °C
BP:
329.4°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
225.449g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
223.92g/mol
Monoisotopic Mass:
223.92g/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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,3,5-Trichlorobenzoic acid is a versatile compound commonly utilized in chemical synthesis. Due to its unique molecular structure and properties, this compound serves as a key building block for the creation of various chemical compounds with specialized functionalities. In organic synthesis, 2,3,5-Trichlorobenzoic acid can be employed as a precursor in the formation of complex organic molecules through a series of chemical reactions such as esterification, amidation, and nucleophilic substitution. Its strategic placement of chlorine atoms on the benzene ring allows for selective functionalization, making it a valuable tool in designing and synthesizing pharmaceuticals, agrochemicals, and advanced materials. Additionally, the presence of electron-withdrawing chlorine groups enhances the reactivity of 2,3,5-Trichlorobenzoic acid, enabling precise control over the regioselectivity and stereochemistry of the desired products. In summary, the strategic incorporation of 2,3,5-Trichlorobenzoic acid in chemical synthesis facilitates the development of novel compounds with tailored properties and applications.