structure of 2-(Aminomethyl)benzoic acid hydrochloride

2-(Aminomethyl)benzoic acid hydrochloride

CAS No.: 10017-39-7
M. Wt: 187.62300
M. Fa: C8H10ClNO2
InChI Key: HWHUNDJAGYQZHL-UHFFFAOYSA-N
Appearance: White Solid

Names and Identifiers of 10017-39-7

CAS Number

10017-39-7

EC Number

695-429-9

MDL Number

MFCD09028989

IUPAC Name

2-(aminomethyl)benzoic acid;hydrochloride

InChI

InChI=1S/C8H9NO2.ClH/c9-5-6-3-1-2-4-7(6)8(10)11;/h1-4H,5,9H2,(H,10,11);1H

InChIKey

HWHUNDJAGYQZHL-UHFFFAOYSA-N

Canonical SMILES

C1=CC=C(C(=C1)CN)C(=O)O.Cl

UNSPSC Code

12352100

Physical and chemical properties of 10017-39-7

Exact Mass

187.04000

LogP

2.34580

Melting Point

219-225°C

Molecular Formula

C8H10ClNO2

Molecular Weight

187.62300

PSA

63.32000

Storage condition

Inert atmosphere,Room Temperature

Safety Information of 10017-39-7

Pictograms

Signal Word

Danger

Safety Data Sheet

Supports customized editing of SDS information and downloading in PDF documents.

Applications of 10017-39-7

2-(Aminomethyl)benzoic acid hydrochloride finds applications in various fields:

  • Pharmaceutical Industry: It serves as an intermediate in the synthesis of various drugs and bioactive compounds.
  • Biochemical Research: Used in studies involving enzyme inhibition and receptor interactions.
  • Chemical Synthesis: Acts as a building block for synthesizing more complex organic molecules.

Its versatility makes it valuable in both academic research and industrial applications.

Interaction Studies of 10017-39-7

Research has indicated that 2-(Aminomethyl)benzoic acid hydrochloride interacts with several biological targets:

  • Proteolytic Enzymes: As mentioned earlier, it acts as a competitive inhibitor, which could be useful in designing therapeutic agents targeting proteases.
  • Receptors: Studies suggest potential interactions with neurotransmitter receptors, indicating possible implications in neuropharmacology.

Further interaction studies are essential to elucidate its full pharmacological profile.

Biological Activity of 10017-39-7

2-(Aminomethyl)benzoic acid hydrochloride has demonstrated various biological activities, including:

  • Enzyme Inhibition: It acts as a competitive inhibitor for certain proteolytic enzymes, which may have implications in therapeutic contexts.
  • Antimicrobial Properties: Some studies suggest that derivatives of this compound exhibit antimicrobial activity, making it a candidate for further pharmacological exploration.
  • Neuroprotective Effects: Preliminary research indicates potential neuroprotective effects, although more studies are needed to substantiate these claims.

Physical sample testing spectrum (NMR) of 10017-39-7

Physical sample testing spectrum (NMR) of 10017-39-7

Retrosynthesis analysis of 10017-39-7

  • Route#1

    Cas:53663-18-6
    Cas:10017-39-7
  • Route#2

    Cas:3839-22-3
    Cas:10017-39-7
  • Route#3

    Cas:85-41-6
    Cas:10017-39-7