structure of 3-(4-bromo-3-methyl-1H-pyrazol-1-yl)propan-1-amine

3-(4-bromo-3-methyl-1H-pyrazol-1-yl)propan-1-amine

CAS No.: 1000802-71-0
M. Wt: 218.09400
M. Fa: C7H12BrN3
InChI Key: PXLXYGZGMUHEBV-UHFFFAOYSA-N
Appearance: Liquid

Names and Identifiers of 1000802-71-0

CAS Number

1000802-71-0

MDL Number

MFCD03422555

IUPAC Name

3-(4-bromo-3-methylpyrazol-1-yl)propan-1-amine

InChI

InChI=1S/C7H12BrN3/c1-6-7(8)5-11(10-6)4-2-3-9/h5H,2-4,9H2,1H3

InChIKey

PXLXYGZGMUHEBV-UHFFFAOYSA-N

Canonical SMILES

CC1=NN(C=C1Br)CCCN

UNSPSC Code

12352100

Physical and chemical properties of 1000802-71-0

Exact Mass

217.02100

LogP

2.00310

Molecular Formula

C7H12BrN3

Molecular Weight

218.09400

PSA

43.84000

Safety Information of 1000802-71-0

Pictograms

Signal Word

Danger

Safety Data Sheet

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

Applications of 1000802-71-0

3-(4-bromo-3-methyl-1H-pyrazol-1-yl)propan-1-amine has several scientific research applications:

  • Chemistry: It serves as a building block in synthesizing more complex molecules.
  • Biology: The compound is explored for its potential antimicrobial and anticancer properties.
  • Medicine: It is investigated as a lead compound for drug development.
  • Industry: Utilized in developing new materials and chemical processes.

Interaction Studies of 1000802-71-0

Interaction studies involving 3-(4-bromo-3-methyl-1H-pyrazol-1-yl)propan-1-amine focus on its binding affinities and effects on various biological targets. These studies help elucidate how the compound modulates biological pathways and its potential therapeutic applications. Specific interactions with enzymes or receptors are crucial for understanding its mechanism of action.

Biological Activity of 1000802-71-0

Research indicates that 3-(4-bromo-3-methyl-1H-pyrazol-1-yl)propan-1-amine exhibits potential biological activities. It has been investigated for its antimicrobial properties and its ability to inhibit certain cancer cell lines. The mechanism of action likely involves binding to specific enzymes or receptors, modulating their activity, which can lead to therapeutic effects.