1-Boc-3-pyrrolidinecarbaldehyde is a chemical compound characterized by its pyrrolidine ring structure, which is a five-membered nitrogen-containing heterocycle. The "Boc" (tert-butyloxycarbonyl) group is a common protecting group used in organic synthesis, particularly in the protection of amines. This compound features an aldehyde functional group, which is reactive and can participate in various chemical reactions, such as condensation and reduction. The presence of both the Boc group and the aldehyde makes it a versatile intermediate in the synthesis of more complex molecules, particularly in the field of medicinal chemistry. Its molecular structure contributes to its solubility in organic solvents, and it is typically handled under standard laboratory conditions. The compound is used in the synthesis of various pharmaceuticals and biologically active compounds, making it significant in research and development. Safety precautions should be observed when handling this compound, as with many organic chemicals, due to potential reactivity and toxicity.

1-Boc-3-pyrrolidinecarbaldehyde

59379-02-1: N-Boc-3-formylpyrrolidine, 3-Formyl-pyrrolidine-1-carboxylic acid tert-butyl ester, tert-Butyl 3-formylpyrrolidine-1-carboxylate, 1-Boc-3-formyl-pyrrolidine

1-Boc-3-formyl-pyrrolidine is a catalytic hydrogenation catalyst that is used in the synthesis of tert-butyl compounds. The 1-Boc group can be removed by catalytic hydrogenation, and the tert-butyl group can be cleaved with diethyl chloroformate to yield the desired product. This catalyst has been shown to have a high efficiency in catalytic hydrogenation reactions and is used in organic synthesis.

CAS 59379-02-1: 1-Boc-3-pyrrolidinecarbaldehyde

1-Boc-3-formyl-pyrrolidine

Ref: 3D-FB50821

1-Boc-Pyrrolidine-3-carboxaldehyde

Ref: 10-F045319

(±)-1-(tert-Butoxycarbonyl)pyrrolidine-3-carboxaldehyde

Ref: 3B-B6091

1-Boc-3-Pyrrolidinecarbaldehyde

Ref: IN-DA0032OY

3-Formylpyrrolidine, N-BOC protected

Ref: 54-OR313035