6-Methoxybenzo[b]thiophene-2-carbaldehyde
Names and Identifiers of 1001203-26-4
CAS Number |
1001203-26-4 |
|---|---|
MDL Number |
MFCD11101038 |
IUPAC Name |
6-methoxy-1-benzothiophene-2-carbaldehyde |
InChI |
InChI=1S/C10H8O2S/c1-12-8-3-2-7-4-9(6-11)13-10(7)5-8/h2-6H,1H3 |
InChIKey |
VHVRCXIIFVHBFI-UHFFFAOYSA-N |
Canonical SMILES |
COC1=CC2=C(C=C1)C=C(S2)C=O |
UNSPSC Code |
12352100 |
Physical and chemical properties of 1001203-26-4
Exact Mass |
192.02500 |
|---|---|
LogP |
2.72240 |
Molecular Formula |
C10H8O2S |
Molecular Weight |
192.23400 |
PSA |
54.54000 |
Safety Information of 1001203-26-4
Applications of 1001203-26-4
6-Methoxybenzo[b]thiophene-2-carbaldehyde serves as a building block in organic synthesis for constructing more complex molecules. Its applications extend to:
- Chemistry: Used in the synthesis of various organic compounds.
- Biology: Investigated for potential therapeutic uses due to its biological activities.
- Industry: Employed in producing dyes, pigments, and other industrial chemicals.
Interaction Studies of 1001203-26-4
The interactions of 6-Methoxybenzo[b]thiophene-2-carbaldehyde with biological targets are under investigation. For instance, its antimicrobial activity may involve disrupting microbial cell membranes or inhibiting specific enzymes crucial for microbial survival. Ongoing studies aim to elucidate these mechanisms further, which could lead to new therapeutic applications.
Biological Activity of 1001203-26-4
Research indicates that 6-Methoxybenzo[b]thiophene-2-carbaldehyde exhibits potential biological activities, particularly antimicrobial and anti-inflammatory properties. Its mechanism of action may involve interactions with microbial cell membranes or specific enzymes involved in inflammatory pathways. Studies are ongoing to explore its efficacy in drug development for various diseases, highlighting its importance in medicinal chemistry.
Physical sample testing spectrum (NMR) of 1001203-26-4
