2-(Benzo[b]thiophen-7-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS No.:
1000160-74-6
M. Wt:
260.16000
M. Fa:
C14H17BO2S
InChI Key:
PNPHOIZEFCAWEB-UHFFFAOYSA-N
Appearance:
Solid
Names and Identifiers of 1000160-74-6
CAS Number |
1000160-74-6 |
|---|---|
MDL Number |
MFCD16995819 |
IUPAC Name |
2-(1-benzothiophen-7-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane |
InChI |
InChI=1S/C14H17BO2S/c1-13(2)14(3,4)17-15(16-13)11-7-5-6-10-8-9-18-12(10)11/h5-9H,1-4H3 |
InChIKey |
PNPHOIZEFCAWEB-UHFFFAOYSA-N |
Canonical SMILES |
B1(OC(C(O1)(C)C)(C)C)C2=C3C(=CC=C2)C=CS3 |
UNSPSC Code |
12352100 |
Physical and chemical properties of 1000160-74-6
Exact Mass |
260.10400 |
|---|---|
H Bond Acceptors |
2 |
H Bond Donors |
0 |
LogP |
3.20050 |
Molecular Formula |
C14H17BO2S |
Molecular Weight |
260.16000 |
PSA |
46.70000 |
Safety Information of 1000160-74-6
Applications of 1000160-74-6
This compound has potential applications in various fields:
- Organic Synthesis: It serves as a versatile building block in the synthesis of complex organic molecules.
- Materials Science: Its unique properties make it suitable for developing new materials with specific functionalities.
- Pharmaceuticals: Given its biological activity potential, it may be explored in drug development processes.
Interaction Studies of 1000160-74-6
Interaction studies involving 2-(Benzo[b]thiophen-7-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane focus on its reactivity with other chemical species. These studies help elucidate its role in catalysis and its behavior in biological systems. Investigations into its interactions with proteins or nucleic acids could provide insights into its potential therapeutic applications.
