1-(3,4-Dimethylphenyl)piperazine, with the CAS number 1014-05-7, is an organic compound that belongs to the piperazine class of chemicals. It features a piperazine ring, which is a six-membered heterocyclic structure containing two nitrogen atoms, and is substituted with a 3,4-dimethylphenyl group. This substitution contributes to its unique chemical properties and potential biological activity. The compound is typically characterized by its moderate solubility in organic solvents and relatively low solubility in water, which is common for many piperazine derivatives. It may exhibit various pharmacological effects, making it of interest in medicinal chemistry and drug development. The presence of the dimethylphenyl group can influence its interaction with biological targets, potentially affecting its efficacy and safety profile. As with many piperazine derivatives, it is important to consider its structure-activity relationship when evaluating its potential applications in pharmaceuticals or other fields. Safety data should be consulted for handling and usage, as with any chemical substance.

1-(3,4-Dimethylphenyl)piperazine

1014-05-7: 1-(3,4-Xylyl)piperazine, 2-(3,4-Dimethylphenyl)Piperidine, 4-(3,4-Dimethylphenyl)Piperazin-1-Ium, 4-(3,4-Dimethylphenyl)piperazine, N-(3,4-Dimethylphenyl)piperazine, N-3,4-Xylylpiperazine, Piperazine, 1-(3,4-dimethylphenyl)-, Piperazine, 1-(3,4-xylyl)-, 1-(3,4-Dimethylphenyl)piperazine

Piperazine, 1-(3,4-dimethylphenyl)-

1-(3,4-Dimethylphenyl)piperazine is a chiral building block for the synthesis of polysubstituted piperazines. It can be used as a bridgehead to synthesize asymmetric amines. The enantioselectivity and yields are high when 1-(3,4-dimethylphenyl)piperazine is used in the ring-opening reaction with an aliphatic allylic amine. This reaction is also efficient with nucleophiles such as primary amines or alcohols.

CAS 1014-05-7: 1-(3,4-Dimethylphenyl)piperazine

Piperazine, 1-(3,4-dimethylphenyl)-

Ref: IN-DA0004F3

1-(3,4-Dimethylphenyl)piperazine

Ref: 3D-BAA01405