α-Methyl-1-piperazineethanol, with the CAS number 1074-54-0, is an organic compound characterized by its piperazine ring structure, which is a six-membered ring containing two nitrogen atoms. This compound features a hydroxyl group (-OH) and a methyl group attached to the piperazine, contributing to its unique properties. It is typically a colorless to pale yellow liquid with a moderate boiling point and is soluble in water due to the presence of the hydroxyl group, which enhances its polarity. α-Methyl-1-piperazineethanol is known for its potential applications in pharmaceuticals and as a building block in organic synthesis. Its basicity is influenced by the piperazine moiety, allowing it to act as a weak base. Additionally, it may exhibit biological activity, making it of interest in medicinal chemistry. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance. Overall, its structural features and functional groups make it a versatile compound in various chemical applications.

α-Methyl-1-piperazineethanol

1074-54-0: 1-(2-Hydroxypropyl)piperazine, 1-(Piperazin-1-Yl)Propan-2-Ol, 1-Methyl-2-(1-piperazinyl)ethanol, 1-Piperazineethanol, α-methyl-, 1074-54-0, 2-Propanol, 1-(1-piperazinyl)-, 4-(2-Hydroxypropyl)piperazine, N-(2-Hydroxypropyl)piperazine, NSC 86963, α-Methyl-1-piperazineethanol

1-(1-piperazinyl)-2-propanol

1-Piperazineethanol, a-methyl-

1-(Piperazin-1-yl)propan-2-ol is a piperazine derivative that has been shown to have cardiotonic activity. It may be used as an antiarrhythmic agent, antihypertensive, or antianginal drug. 1-(Piperazin-1-yl)propan-2-ol binds to the L type calcium channel in heart muscle cells and prevents calcium from entering the cell. This binding inhibits depolarization of the cell membrane and reduces the strength of contractions.

CAS 1074-54-0: α-Methyl-1-piperazineethanol

1-(1-piperazinyl)-2-propanol

Ref: 10-F313029

1-Piperazineethanol, a-methyl-

Ref: IN-DA0084P4

1-(Piperazin-1-yl)propan-2-ol

Ref: 3D-FP178650