structure of 4-Bromothiophene-3-carboxamide

4-Bromothiophene-3-carboxamide

CAS No.: 100245-61-2
M. Wt: 206.06000
M. Fa: C5H4BrNOS
InChI Key: BMZBDWPOBVGKSU-UHFFFAOYSA-N
Appearance: White Solid

Names and Identifiers of 4-Bromothiophene-3-carboxamide

CAS Number

100245-61-2

EC Number

664-259-7

MDL Number

MFCD17171292

IUPAC Name

4-bromothiophene-3-carboxamide

InChI

InChI=1S/C5H4BrNOS/c6-4-2-9-1-3(4)5(7)8/h1-2H,(H2,7,8)

InChIKey

BMZBDWPOBVGKSU-UHFFFAOYSA-N

Canonical SMILES

C1=C(C(=CS1)Br)C(=O)N

UNSPSC Code

12352100

Physical and chemical properties of 4-Bromothiophene-3-carboxamide

Exact Mass

204.92000

LogP

2.30980

Melting Point

150-155°C

Molecular Formula

C5H4BrNOS

Molecular Weight

206.06000

PSA

71.33000

Storage condition

2-8°C(protect from light)

Safety Information of 4-Bromothiophene-3-carboxamide

Pictograms

Signal Word

Warning

Safety Data Sheet

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

Applications of 4-Bromothiophene-3-carboxamide

4-Bromothiophene-3-carboxamide has several applications:

  • Pharmaceuticals: It is being investigated for its potential as an active pharmaceutical ingredient due to its biological properties.
  • Materials Science: Its unique electronic properties make it suitable for use in organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics.
  • Chemical Intermediates: It serves as a building block for synthesizing more complex organic molecules.

Interaction Studies of 4-Bromothiophene-3-carboxamide

Interaction studies involving 4-Bromothiophene-3-carboxamide focus on its reactivity with various biological targets. Preliminary research suggests that it may interact with proteins involved in cellular signaling pathways, potentially influencing processes such as cell proliferation and apoptosis. Further studies are needed to elucidate these interactions and their implications for therapeutic applications.

Biological Activity of 4-Bromothiophene-3-carboxamide

The biological activity of 4-Bromothiophene-3-carboxamide has been explored in various studies. Thiophene derivatives are known for their antimicrobial and antifungal properties, and compounds similar to 4-bromothiophene-3-carboxamide have shown promise as potential drug candidates in treating infections. Additionally, some studies indicate that thiophene-based compounds exhibit anti-inflammatory and anticancer activities, although specific data on 4-bromothiophene-3-carboxamide remains limited.

Physical sample testing spectrum (NMR) of 4-Bromothiophene-3-carboxamide

Physical sample testing spectrum (NMR) of 4-Bromothiophene-3-carboxamide

Retrosynthesis analysis of 4-Bromothiophene-3-carboxamide

  • Route#1

    Cas:16694-17-0
    Cas:100245-61-2
  • Route#2

    Cas:18791-95-2
    Cas:100245-61-2
  • Route#3

    Cas:18895-10-8
    Cas:100245-61-2