876-03-9 | 3-(Aminomethyl)benzoic acid, HCl

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$6.00	$4.00
250mg	97%	in stock	$7.00	$5.00
1g	95%	in stock	$19.00	$13.00
5g	95%	in stock	$60.00	$42.00
10g	95%	in stock	$72.00	$51.00

Description

• Catalog Number: AB52344
• Chemical Name: 3-(Aminomethyl)benzoic acid, HCl
• CAS Number: 876-03-9
• Molecular Formula: C8H10ClNO2
• Molecular Weight: 187.6235
• MDL Number: MFCD03791117
• SMILES: NCc1cccc(c1)C(=O)O.Cl

Computed Properties

• Complexity: 147
• Covalently-Bonded Unit Count: 2
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 2

Upstream Synthesis Route

The 3-(Aminomethyl)benzoic acid hydrochloride is a versatile compound widely utilized in chemical synthesis. Amino acids are crucial building blocks in organic chemistry, and this particular compound provides a key intermediate for the synthesis of various biologically active molecules. One common application of 3-(Aminomethyl)benzoic acid hydrochloride is in the preparation of peptides and pharmaceutical drugs. By reacting this compound with other amino acids or peptide fragments, chemists can synthesize complex peptides with specific structures and functions. This is particularly important in the development of new drugs and therapeutic agents.Furthermore, 3-(Aminomethyl)benzoic acid hydrochloride can also be used in the synthesis of various polymers and materials. Its unique chemical properties make it a valuable precursor in the production of specialty polymers with specific properties such as biodegradability, conductivity, or thermal stability.In addition to its role in peptide and polymer synthesis, 3-(Aminomethyl)benzoic acid hydrochloride can also be employed in the preparation of dyes, pigments, and other fine chemicals. Its versatility and reactivity make it a valuable tool for chemists working in various fields of chemical research and development.

Literature

• Synthesis and evaluation of novel aromatic substrates and competitive inhibitors of GABA aminotransferase.

  Bioorganic & medicinal chemistry letters 20080515