Interesting facts
Interesting Facts about Benzothiophen-4-yl N-methylcarbamate
Benzothiophen-4-yl N-methylcarbamate is a fascinating compound known for its unique structure and intriguing properties. Here are some notable aspects of this compound:
- Chemical Structure: The compound features a benzothiophene ring, which contributes to its aromatic character and electronic stability. Benzothiophenes are known for their role in organic electronics and photochemistry.
- Biological Relevance: Compounds of this class have shown potential in various biological activities. Research indicates that derivatives can exhibit herbicidal and insecticidal properties, making them significant in agrochemicals.
- Pharmaceutical Applications: Benzothiophenes are often explored for their therapeutic benefits. The N-methylcarbamate moiety can enhance the bioavailability of these compounds, leading to increased efficacy in medicinal chemistry.
- Environmental Impact: Understanding the fate of such compounds in the environment is crucial. Studies on their degradation pathways can inform on their persistence and ecological risks.
- Synthesis Challenges: The synthesis of benzothiophen-4-yl N-methylcarbamate may involve multiple steps, including functionalization of the benzothiophene precursor. This provides a stimulating challenge for chemists in developing synthetic methodologies.
- Research Potential: The continuous exploration of benzothiophen derivatives can lead to novel discoveries in materials science, particularly in organic semiconductors and photovoltaic devices.
In summary, benzothiophen-4-yl N-methylcarbamate presents numerous avenues for both academic research and practical applications, illustrating the importance of studying and understanding this fascinating compound.
Synonyms
MOBAM
Mobam phenol
4-Benzothienyl methylcarbamate
4-Benzothienyl N-methyl-carbamate
Caswell No. 081D
OMS-708
Benzo(b)thiophene-4-ol, methylcarbamate
1-benzothiophen-4-yl N-methylcarbamate
Benzo[b]thiophene-4-ol, methylcarbamate
HSDB 1515
Benzo(b)thien-4-yl methylcarbamate
UNII-8M3AR1XD9I
MC-A-600
EPA Pesticide Chemical Code 090401
BRN 1427973
4-benzothienyl N-methylcarbamate
AI3-27041
4-Benzothienylester kyseliny methylkarbaminove
MOBAM [HSDB]
Carbamic acid, methyl-, benzo(b)thien-4-yl ester
Carbamic acid, methyl-, benzo[b]thien-4-yl ester
4-Benzothienylester kyseliny methylkarbaminove [Czech]
DTXSID0042161
MCA 600
1-Benzothien-4-yl methylcarbamate
Benzo[b]thien-4-yl methylcarbamate
BENZO(B)THIOPHENE-4-OL, 4-(N-METHYLCARBAMATE)
4-Benzothienylester kyseliny methylkarbaminove (Czech)
DTXCID8022161
USEPA/OPP Pesticide Code: 90401
5-17-04-00199 (beilstein handbook reference)
botuvxisjhkzkj-uhfffaoysa-n
1079-33-0
Mobil MC-A-600
MOS-708
ENT-27041
MCA-600
benzo[b]thiophen-4-yl methylcarbamate
8M3AR1XD9I
starbld0002292
Benzo[b]thiophene-4-ol,4-(N-methylcarbamate)
SCHEMBL5934013
1-Benzothien-4-yl methylcarbamate #
1-benzothiophen-4-yl methylcarbamate
STL430455
AKOS037479280
HY-126021
NS00120474
AO-365/43506489
Q27270739
Solubility of Benzothiophen-4-yl N-methylcarbamate
Benzothiophen-4-yl N-methylcarbamate, a compound belonging to the carbamate family, exhibits intriguing solubility characteristics:
In summary, the solubility of benzothiophen-4-yl N-methylcarbamate is quite versatile and influenced by several factors including solvent type, pH level, and temperature. Understanding these solubility traits is crucial for applications in chemical synthesis and formulation processes.