Central nervous system drugs

N , N -diisopropylethylamine is an aliphatic sterically hindered amine. Application N , N -diisopropylethylamine may be used in the following processes: As an organic base in the synthesis of indenopyrones.

N , N -diisopropylethylamine is an aliphatic sterically hindered amine. Application N , N -diisopropylethylamine may be used in the following processes: As an organic base in the synthesis of indenopyrones.

N , N -diisopropylethylamine is an aliphatic sterically hindered amine. Application N , N -diisopropylethylamine may be used in the following processes: As an organic base in the synthesis of indenopyrones.

N , N -Diisopropylethylamine is a hindered non-nucleophilic amine base used in alkylation, aldol-like reactions, eliminations, and selective generation of enolates. It is widely used as a proton scavenger in organic synthesis.

N , N -Diisopropylethylamine is a hindered non-nucleophilic amine base used in alkylation, aldol-like reactions, eliminations, and selective generation of enolates. It is widely used as a proton scavenger in organic synthesis.

Application ZerO2 products are rigorously degassed with highly pure inert gas providing solvents and solutions (anhydrous if specified) with very low residual oxygen content. Legal Information ZerO 2 &#174 is a trademark of Sigma-Aldrich Co.

N,N -Diisopropylethylamine, also known as Hünig&#8242s base, is a sterically hindered amine. It is a non-nucleophilic base commonly employed for substitution reactions.

N,N -Diisopropylethylamine, also known as Hünig&#8242s base, is a sterically hindered amine. It is a non-nucleophilic base commonly employed for substitution reactions.

N,N -Diisopropylethylamine, also known as Hünig&#8242s base, is a sterically hindered amine. It is a non-nucleophilic base commonly employed for substitution reactions.

N,N -Diisopropylethylamine, also known as Hünig&#8242s base, is a sterically hindered amine. It is a non-nucleophilic base commonly employed for substitution reactions.

N,N -Diisopropylethylamine, also known as Hünig&#8242s base, is a sterically hindered amine. It is a non-nucleophilic base commonly employed for substitution reactions.

N，N-Dimethyl-1，3，5-triazine-2，4-diamine.