3-Hydroxybenzylamine - ≥97% , CAS No.73604-31-6

CAS: 73604-31-6 Cat. No.: H407384 Formule: C₇H₉NO Poids moléculaire: 123.15 Numéro CE: 674-286-6

GRADE & PURITY ≥97%

Synonyms

3-Hydroxybenzylamine | 3-hydroxy-benzylamine | A837869 | 3-aminomethyl-phenol | SCHEMBL138953 | 3-Aminomethyl phenol | Phenol, 3-(aminomethyl)- | BRD-K63116520-001-01-2 | CHEBI:125604 | NoName_3499 | MFCD00798977 | DTXSID90902923 | SY005415 | 3-(aminometh

Storage

Store at 2-8°C,Protected from light,Argon charged

Shipped In

Wet ice

Vue d’ensemble

Product Application:

3-Hydroxybenzylamine is used as pharmaceutical intermediate.

Specifications

Synonymes

3-Hydroxybenzylamine | 3-hydroxy-benzylamine | A837869 | 3-aminomethyl-phenol | SCHEMBL138953 | 3-Aminomethyl phenol | Phenol, 3-(aminomethyl)- | BRD-K63116520-001-01-2 | CHEBI:125604 | NoName_3499 | MFCD00798977 | DTXSID90902923 | SY005415 | 3-(aminometh

Spécifications et pureté

≥97%

Conditions de stockage de stockage

Store at 2-8°C,Protected from light,Argon charged

Expédié en

Wet ice

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Type d'action

INHIBITOR

Pureté

≥97%

Noms et identifiants

• Pubchem Sid: 528758654
• Sourires canoniques: C1=CC(=CC(=C1)O)CN
• IUPAC Name: 3-(aminomethyl)phenol
• InChIKey: JNZYADHPGVZMQK-UHFFFAOYSA-N
• INCHI: 1S/C7H9NO/c8-5-6-2-1-3-7(9)4-6/h1-4,9H,5,8H2
• Isomères SMILES: C1=CC(=CC(=C1)O)CN
• Poids moléculaire: 123.15
• Reaxy-Rn: 2802320
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2802320&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Phenylmethylamines

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Phenylmethylamines
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenylmethylamines
• Alternative Parents: Benzylamines Aralkylamines 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Organopnictogen compounds Organooxygen compounds Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Benzylamine - Phenylmethylamine - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Aralkylamine - Amine - Hydrocarbon derivative - Primary amine - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organic nitrogen compound - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as phenylmethylamines. These are compounds containing a phenylmethtylamine moiety, which consists of a phenyl group substituted by an methanamine.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: Soluble in water and ethanol.
• Sensibilité: Light and moisture sensitive；Air sensitive
• Point de fusion (°C): 165-168
• Poids moléculaire: 123.150 g/mol
• XLogP3: 0.200
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 123.068 Da
• Monoisotopic Mass: 123.068 Da
• Topological Polar Surface Area: 46.300 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 85.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Références

1. Hongyu Chen, Jiayi Guo, Xinrui Sun, Peipei Tian, Wenping Zhu, Manman Sun, Zengchen Liu, Qingfeng Li, Yahong Chen.  (2026)  Analyte-guided precise regulation of gold nanoflower etching mechanism for enhanced dopamine selectivity via bisphenol-triggered Schiff base/Michael addition and intramolecular hydrogen bond synergy.  TALANTA,      [PMID:41558403] [10.1016/j.talanta.2026.129412]