CAS 21483-64-7: Carbamic acid, (2-bromo-3-thienyl)-, 1,1-dimethylethyl ester

Description: Carbamic acid, (2-bromo-3-thienyl)-, 1,1-dimethylethyl ester, with the CAS number 21483-64-7, is an organic compound characterized by its ester functional group derived from carbamic acid. This compound features a thienyl ring, which is a five-membered aromatic heterocycle containing sulfur, and a bromine substituent at the 2-position, contributing to its reactivity and potential biological activity. The presence of the tert-butyl group (1,1-dimethylethyl) enhances its lipophilicity, which may influence its solubility and interaction with biological membranes. The compound's structure suggests potential applications in agrochemicals or pharmaceuticals, particularly in the development of herbicides or insecticides, due to the thienyl moiety's known activity in these areas. Additionally, the bromine atom may impart unique properties, such as increased electrophilicity or the ability to participate in further chemical reactions. As with many organic compounds, safety and handling precautions should be observed, given the potential hazards associated with brominated compounds.

Formula: C₉H₁₂BrNO₂S

tert-butyl (2-broMothiophen-3-yl)carbaMate

CAS: 21483-64-7

• Formula: C₉H₁₂BrNO₂S
• Purity: 97%
• Color and Shape: Solid
• Molecular weight: 278.1661

tert-Butyl (2-bromothiophen-3-yl)carbamate

CAS: 21483-64-7

• Purity: 95%
• Molecular weight: 278.17g/mol

3-(BOC-AMINO)-2-BROMOTHIOPHENE

CAS: 21483-64-7

• Purity: 97.0%
• Color and Shape: Solid, White to Yellow Solid
• Molecular weight: 278.1600036621094

3-(Boc-amino)-2-bromothiophene

CAS: 21483-64-7

Versatile small molecule scaffold

• Formula: C₉H₁₂BrNO₂S
• Purity: Min. 95%
• Molecular weight: 278.17 g/mol