CAS 5514-98-7
:Hexanoic acid, 6-amino-, 1,1-dimethylethyl ester
Description:
Hexanoic acid, 6-amino-, 1,1-dimethylethyl ester, also known by its CAS number 5514-98-7, is an organic compound characterized by its ester functional group derived from hexanoic acid and 6-amino-1,1-dimethylethanol. This compound typically appears as a colorless to pale yellow liquid with a characteristic odor. It is soluble in organic solvents and exhibits moderate polarity due to the presence of both hydrophobic (hexanoic acid) and hydrophilic (amino group) components. The presence of the amino group suggests potential for hydrogen bonding, which can influence its reactivity and interactions with other molecules. Hexanoic acid derivatives are often used in various applications, including as intermediates in the synthesis of pharmaceuticals, agrochemicals, and surfactants. Safety data indicates that, like many organic compounds, it should be handled with care, as it may cause irritation upon contact with skin or eyes. Proper storage and handling protocols are essential to ensure safety and stability.
Formula:C10H21NO2
Synonyms:- 6-Aminohexanoic acid tert-butyl ester
- tert-butyl 6-aminohexanoate
- tert-Butyl 6-aminocaproate
- Hexanoic acid, 6-amino-, 1,1-dimethylethyl ester
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Found 3 products.
tert-Butyl 6-aminohexanoate
CAS:<p>tert-Butyl 6-aminohexanoate is a benzene derivative that is used as a spacer in organic synthesis. It reacts with potassium carbonate to form tert-butyl 6-aminocaproate and tert-butyl 2,6-dinitrophenolate. The tert-butyl group has an amino group at one end and a carboxylic acid group at the other end. This tertiary amine is made by reacting benzene with potassium hydroxide and adding 1-4c alkyl chloride. The tertiary amine functional group is reactive towards electrophilic aromatic substitution reactions, such as nitration or halogenation.</p>Formula:C10H21NO2Purity:Min. 95%Molecular weight:187.28 g/mol
