CAS 93483-71-7

N-tert-Butyl-4-aminobenzamide

Description:

N-tert-Butyl-4-aminobenzamide is an organic compound characterized by its amide functional group and a tert-butyl substituent. It features a benzene ring with an amino group (-NH2) and a tert-butyl group attached to the para position relative to the amine. This structure contributes to its unique chemical properties, including increased lipophilicity due to the bulky tert-butyl group, which can influence its solubility and reactivity. The compound is typically a solid at room temperature and may exhibit moderate stability under standard conditions. Its amine group can participate in hydrogen bonding, affecting its interactions with other molecules. N-tert-Butyl-4-aminobenzamide may be utilized in various applications, including pharmaceuticals and organic synthesis, where it can serve as a building block or intermediate. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken.

Formula: C₁₁H₁₆N₂O

InChI: InChI=1S/C11H16N2O/c1-11(2,3)13-10(14)8-4-6-9(12)7-5-8/h4-7H,12H2,1-3H3,(H,13,14)

InChI key: InChIKey=IBSCJDKXUQIEPQ-UHFFFAOYSA-N

SMILES: C(NC(C)(C)C)(=O)C1=CC=C(N)C=C1

Synonyms:

• N-tert-Butyl-4-aminobenzamide
• Benzamide, 4-amino-N-(1,1-dimethylethyl)-
• 4-Amino-N-(tert-butyl)benzamide
• 4-Amino-N-(1,1-dimethylethyl)benzamide
• Benzamide, p-amino-N-tert-butyl-

4-Amino-N-(tert-butyl)benzamide

CAS: 93483-71-7

4-Amino-N-(tert-butyl)benzamide

Purity: 98%

Molecular weight: 192.26g/mol

Ref: 54-OR1074096

4-Amino-n-tert-butylbenzamide

CAS: 93483-71-7

Purity: 98%

Molecular weight: 192.2619934

Ref: 10-F660015

4-Amino-N-(tert-butyl)benzamide

CAS: 93483-71-7

4-Amino-N-(tert-butyl)benzamide is a chemical intermediate that can be used in the preparation of certain pharmaceuticals. This compound is synthesized through the reaction of 4-aminobenzoyl chloride and tert-butanol, which forms an amide bond. The condensation reaction can be catalyzed by either heat or acid. The product of this reaction is hydrogenated to form 4-amino-N-(tert-butyl)-N'-(chloromethyl)benzamide. This compound can also be prepared by refluxing a mixture of 4-aminobenzaldehyde and hydrazine with chloroform and hydrochloric acid.

Formula: C₁₁H₁₆N₂O

Purity: Min. 95%

Molecular weight: 192.26 g/mol

Ref: 3D-TDA48371