5-amino-2-(trifluoromethyl)benzonitrile

5-amino-2-(trifluoromethyl)benzonitrile

4-propylphenylacetic acid

4-propylphenylacetic acid

4-(sec-Butyl)aniline

$250.00
CAS No.: 30273-11-1
Catalog No.: 194075
Purity: 95%
MF: C10H15N
MW: 149.237
Storage: 2-8 degree Celsius
SMILES: C(C)(CC)C1=CC=C(N)C=C1
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194075
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4-(sec-Butyl)aniline; CAS No.: 30273-11-1; 4-(sec-Butyl)aniline. PROPERTIES: 4-(sec-Butyl)aniline is a colorless to pale yellow liquid. Its molecular formula is C10H15N, with a molecular weight of approximately 151.23 g/mol. The compound has a boiling point of around 180-182 C. It is slightly soluble in water but mixes well with most organic solvents such as ethanol and hexane. For stable storage, it should be kept in a tightly sealed container in a cool, dry place, ideally at temperatures below 20 C. As an aromatic amine compound, it may pose certain health risks. When handling it, protective gloves, eye protection, and a lab coat should be worn. In case of skin contact, washing with soap and water is necessary, and in case of eye contact, thorough rinsing with water is required. APPLICATIONS: In organic synthesis, 4-(sec-Butyl)aniline can act as an important intermediate. The amine group can undergo reactions such as acylation, sulfonation, and diazotization. The sec-butyl substituent on the benzene ring provides steric hindrance and specific electronic effects, which can influence the reaction pathways and selectivity. In the dye industry, derivatives of 4-(sec-Butyl)aniline can be used to synthesize dyes with unique colors and properties. For example, by reacting 4-(sec-Butyl)aniline with appropriate diazo compounds, azo dyes with good colorfastness can be obtained (as noted in dye chemistry literature). Additionally, in the field of pharmaceutical research, 4-(sec-Butyl)aniline can be used as a starting material for the synthesis of certain drugs. Its structure can be modified to develop compounds with specific biological activities, such as anti-allergic or anti-inflammatory agents (as described in medicinal chemistry research articles).

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