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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)-

4-[4-(aminomethyl)phenyl]benzoic acid hydrochloride

NCc1ccc(cc1)c1ccc(cc1)C(=O)O.Cl Request for Quotation
Chemical Name: 4-[4-(aminomethyl)phenyl]benzoic acid hydrochloride
CAS Number: 578026-68-3
Product Number: AG01ELL8(AG01ELL8)
Synonyms:
MDL No:
Molecular Formula: C14H14ClNO2
Molecular Weight: 263.7195

Identification/Properties

Computed Properties
Molecular Weight:
263.721g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
263.071g/mol
Monoisotopic Mass:
263.071g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
251
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-[4-(Aminomethyl)phenyl]benzoic acid hydrochloride, commonly known as $name$, is a versatile compound widely utilized in chemical synthesis. This compound plays a crucial role in the development of pharmaceuticals, agrochemicals, and advanced materials due to its unique chemical properties. In chemical synthesis, $name$ is a key intermediate in the preparation of various organic compounds through functional group transformations. Its amino and carboxylic acid groups provide valuable starting points for the introduction of different functional groups, enabling the construction of complex molecular structures. Moreover, the benzoic acid moiety in $name$ serves as a versatile building block for the synthesis of biologically active molecules and novel materials. The hydrochloride salt form of 4-[4-(Aminomethyl)phenyl]benzoic acid enhances its solubility in aqueous media, making it suitable for a wide range of synthetic transformations. In summary, the application of 4-[4-(Aminomethyl)phenyl]benzoic acid hydrochloride in chemical synthesis offers tremendous potential for the efficient and versatile preparation of diverse organic compounds for various industrial and research purposes.