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3,5-Bis(aminomethyl)benzoic acid dihydrochloride

  • CAS No. 185963-32-0

  • Cat. No. CS-0045347
  • Molecule weightNone
  • Purity≥98%
  • MDL No.MFCD28144945

*For research and further manufacturing use only, not for direct human use.

3,5-Bis(aminomethyl)benzoic acid dihydrochloride|CS-0045347

Structure of 185963-32-0

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General Information

  • CAS No. 185963-32-0
  • Cat. No. CS-0045347
  • Purity ≥98%
  • MDL No. MFCD28144945
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₁₄Cl₂N₂O₂
  • Molecular Weight None
  • Synonym(s) 3,5-BIS(AMINOMETHYL)BENZOIC ACID 2HCL
  • SMILES O=C(O)C1=CC(CN)=CC(CN)=C1.[H]Cl.[H]Cl

Description

This bifunctional diacid derivative features two aminomethyl groups flanking a carboxylic acid moiety, enabling efficient conjugation in peptide and polymer synthesis. The dihydrochloride salt enhances solubility and stability under standard handling conditions, facilitating use in solution-phase reactions and solid-phase workflows.

Application

3,5-Bis(aminomethyl)benzoic acid dihydrochloride serves as a versatile bifunctional building block for peptide and macrocyclic scaffold synthesis. The ortho-diaminomethyl functionality enables efficient metal coordination and cyclization reactions, while the carboxylic acid group facilitates conjugation via amide bond formation. Bench-stable and readily purified by recrystallization, it functions effectively in standard coupling protocols and offers high functional group tolerance in multi-step synthetic sequences.

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Computational Chemistry Data

  • TPSA   89.34
  • LogP   1.1458
  • H_Acceptors   3
  • H_Donors   3
  • Rotatable_Bonds   3

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