structure of 3-(4-Bromo-2-methoxyphenyl)propan-1-amine

3-(4-Bromo-2-methoxyphenyl)propan-1-amine

CAS No.: 1000504-26-6
M. Wt: 244.13
M. Fa: C10H14BrNO
InChI Key: OXURAAPXMZEYQC-UHFFFAOYSA-N

Names and Identifiers of 1000504-26-6

CAS Number

1000504-26-6

EC Number

959-014-9

IUPAC Name

3-(4-bromo-2-methoxyphenyl)propan-1-amine

InChI

InChI=1S/C10H14BrNO/c1-13-10-7-9(11)5-4-8(10)3-2-6-12/h4-5,7H,2-3,6,12H2,1H3

InChIKey

OXURAAPXMZEYQC-UHFFFAOYSA-N

Canonical SMILES

COC1=C(C=CC(=C1)Br)CCCN

Physical and chemical properties of 1000504-26-6

Molecular Formula

C10H14BrNO

Molecular Weight

244.13

Safety Information of 1000504-26-6

Pictograms

Signal Word

 Danger

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

Applications of 1000504-26-6

3-(4-Bromo-2-methoxyphenyl)propan-1-amine has several applications across different fields:

  • Chemistry: It serves as an intermediate in the synthesis of more complex organic molecules.
  • Biology: The compound is investigated for its potential interactions with biological receptors, contributing to studies in pharmacology.
  • Medicine: It is explored for therapeutic effects and as a precursor for drug development.
  • Industry: The compound is utilized in producing specialty chemicals and materials.

Interaction Studies of 1000504-26-6

The mechanism of action of 3-(4-Bromo-2-methoxyphenyl)propan-1-amine involves its interaction with specific molecular targets, including receptors and enzymes. The presence of the bromine atom and methoxy group on the benzene ring significantly influences the compound's binding affinity and selectivity towards these targets. Such interactions are essential for understanding its biological activity and potential therapeutic applications.

Biological Activity of 1000504-26-6

Research indicates that 3-(4-Bromo-2-methoxyphenyl)propan-1-amine exhibits potential biological activity. It has been studied for its interactions with biological receptors and enzymes, which may lead to therapeutic applications. The compound's ability to modulate receptor activity makes it a candidate for further exploration in medicinal chemistry.