CAS 130369-09-4

Carbamic acid, [(3-oxocyclobutyl)methyl]-, 1,1-dimethylethyl ester (9CI)

Description:

Carbamic acid, [(3-oxocyclobutyl)methyl]-, 1,1-dimethylethyl ester, with the CAS number 130369-09-4, is an organic compound characterized by its carbamate functional group. This substance features a cyclobutane ring with a ketone substituent, contributing to its unique structural properties. The presence of the tert-butyl ester group enhances its stability and solubility in organic solvents. Typically, carbamic acid derivatives exhibit moderate to low toxicity and can participate in various chemical reactions, including hydrolysis and transesterification. The compound may be utilized in synthetic organic chemistry, particularly in the development of pharmaceuticals or agrochemicals, due to its potential reactivity and ability to form derivatives. Its physical properties, such as boiling point, melting point, and solubility, would depend on the specific molecular interactions and the presence of functional groups. As with many chemical substances, safety data sheets should be consulted for handling and storage guidelines, as well as potential environmental impacts.

Formula: C₁₀H₁₇NO₃

Carbamic acid, [(3-oxocyclobutyl)methyl]-, 1,1-dimethylethyl ester (9CI)

CAS: 130369-09-4

Formula: C₁₀H₁₇NO₃

Purity: 97%

Color and Shape: Solid

Molecular weight: 199.2469

Ref: IN-DA000UBC

3-(Boc-aminomethyl)cyclobutanone

CAS: 130369-09-4

3-(Boc-aminomethyl)cyclobutanone

Formula: C₁₀H₁₇NO₃

Purity: 97%

Color and Shape: white powder

Molecular weight: 199.25g/mol

Ref: 54-OR317084

tert-Butyl ((3-oxocyclobutyl)methyl)carbamate

CAS: 130369-09-4

Formula: C₁₀H₁₇NO₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 199.25

Ref: 10-F465121

3-(Boc-aminomethyl)cyclobutanone

CAS: 130369-09-4

3-(Boc-aminomethyl)cyclobutanone is a biologically active compound that is synthesized by the reaction of trimethylbenzene, benzylamine and hydrochloric acid. It can be used as an inhibitor of enzymes such as carboxypeptidase A, chymotrypsin, and trypsin. 3-(Boc-aminomethyl)cyclobutanone is also synthesized by the reaction of cyclobutanone with tetrahydrofuran catalyzed by sodium methoxide. The prochiral nature of this molecule makes it useful for asymmetric synthesis.

Formula: C₁₀H₁₇NO₃

Purity: Min. 95%

Molecular weight: 199.25 g/mol

Ref: 3D-FFA36909