structure of 5-(benzyloxy)-1H-pyrazol-3-amine

5-(benzyloxy)-1H-pyrazol-3-amine

CAS No.: 1000896-40-1
M. Wt: 189.21400
M. Fa: C10H11N3O
InChI Key: DPMPAHAAODHNKV-UHFFFAOYSA-N
Appearance: Solid

Names and Identifiers of 5-(benzyloxy)-1H-pyrazol-3-amine

CAS Number

1000896-40-1

EC Number

850-626-0

MDL Number

MFCD18205693

IUPAC Name

3-phenylmethoxy-1H-pyrazol-5-amine

InChI

InChI=1S/C10H11N3O/c11-9-6-10(13-12-9)14-7-8-4-2-1-3-5-8/h1-6H,7H2,(H3,11,12,13)

InChIKey

DPMPAHAAODHNKV-UHFFFAOYSA-N

Canonical SMILES

C1=CC=C(C=C1)COC2=NNC(=C2)N

UNSPSC Code

12352100

Physical and chemical properties of 5-(benzyloxy)-1H-pyrazol-3-amine

Acidity coefficient

14.08±0.10(Predicted)

Boiling Point

446.6±30.0 °C(Predicted)

Density

1.278±0.06 g/cm3(Predicted)

Exact Mass

189.09000

LogP

2.15210

Molecular Formula

C10H11N3O

Molecular Weight

189.21400

PSA

63.93000

Storage condition

under inert gas (nitrogen or Argon) at 2–8 °C

Safety Information of 5-(benzyloxy)-1H-pyrazol-3-amine

Pictograms

Signal Word

 Warning

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

Applications of 5-(benzyloxy)-1H-pyrazol-3-amine

5-(Benzyloxy)-1H-pyrazol-3-amine has various applications in:

  • Pharmaceutical Development: It serves as a building block for synthesizing more complex molecules with potential therapeutic effects.
  • Agrochemicals: The compound may be utilized in developing new agricultural chemicals.
  • Specialty Chemicals: It finds use in producing dyes and other industrial products due to its unique chemical properties.

Interaction Studies of 5-(benzyloxy)-1H-pyrazol-3-amine

Studies on 5-(benzyloxy)-1H-pyrazol-3-amine have revealed its ability to interact with specific molecular targets. This interaction can modulate enzyme activity and receptor binding, leading to various biological effects. For instance, it may inhibit certain protein kinases involved in cell signaling pathways.

Biological Activity of 5-(benzyloxy)-1H-pyrazol-3-amine

5-(Benzyloxy)-1H-pyrazol-3-amine exhibits significant biological activity, making it a subject of interest in medicinal chemistry. It may act as an inhibitor for various enzymes and receptors, impacting cellular processes such as proliferation and survival. Its derivatives have been studied for potential therapeutic effects against different diseases, including cancer and inflammatory conditions.