CAS 264600-97-7

Carbamic acid,N-3-isoxazolyl-, 1,1-dimethylethyl ester

Description:

Carbamic acid, N-3-isoxazolyl-, 1,1-dimethylethyl ester, identified by the CAS number 264600-97-7, is an organic compound characterized by its carbamate functional group. This substance features a 3-isoxazolyl moiety, which contributes to its unique chemical properties, including potential biological activity. The presence of the 1,1-dimethylethyl group enhances its steric bulk, influencing its reactivity and solubility. Typically, carbamates like this compound exhibit moderate stability under standard conditions but can be sensitive to hydrolysis, especially in the presence of strong acids or bases. They may also demonstrate varying degrees of lipophilicity, affecting their absorption and distribution in biological systems. The compound's potential applications could span areas such as pharmaceuticals, agrochemicals, or as intermediates in organic synthesis, depending on its specific reactivity and biological interactions. As with many chemical substances, safety data sheets should be consulted for handling and toxicity information, as carbamates can exhibit varying levels of toxicity to humans and the environment.

Formula: C₈H₁₂N₂O₃

Synonyms:

• Carbamicacid, 3-isoxazolyl-, 1,1-dimethylethyl ester (9CI)
• 3-(tert-Butoxycarbonylamino)isoxazole
• Isoxazol-3-ylcarbamic acid tert-butylester
• tert-Butyl isoxazol-3-ylcarbamate

Carbamic acid, N-3-isoxazolyl-, 1,1-dimethylethyl ester

CAS: 264600-97-7

Formula: C₈H₁₂N₂O₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 184.1925

Ref: IN-DA002TBK

tert-Butyl isoxazol-3-ylcarbamate

CAS: 264600-97-7

tert-Butyl isoxazol-3-ylcarbamate

Purity: 97%

Molecular weight: 184.20g/mol

Ref: 54-OR74473

tert-Butyl isoxazol-3-ylcarbamate

CAS: 264600-97-7

Formula: C₈H₁₂N₂O₃

Purity: 98%

Molecular weight: 184.195

Ref: 10-F230060

tert-Butyl isoxazol-3-ylcarbamate

CAS: 264600-97-7

tert-Butyl isoxazol-3-ylcarbamate (TBIC) is a tertiary amine that reacts with electrophiles such as halogens, nitrites, and sulfonates. TBIC reacts efficiently with lithiated isoxazoles to form the corresponding tertiary amides. In contrast to isoxazoles, TBIC does not react with primary and secondary amines. TBIC has been shown to be an efficient catalyst for the synthesis of aminoisoxazoles in high yields.

Formula: C₈H₁₂N₂O₃

Purity: Min. 95%

Molecular weight: 184.2 g/mol

Ref: 3D-PKA60097