(1S,2R)-2-(Methylamino)cyclopentan-1-ol

97%

Reagent Code: #36239
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CAS Number 135969-66-3

science Other reagents with same CAS 135969-66-3

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Weight 115.1700 g/mol
Formula C₆H₁₃NO
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Storage room temperature

description Product Description

This compound is primarily used in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) drugs. Its structure, featuring a cyclopentane ring with hydroxyl and methylamino groups, makes it a valuable intermediate in creating molecules that interact with neurotransmitter systems. It is often utilized in the production of compounds targeting adrenergic and dopaminergic receptors, which are critical in treating conditions like Parkinson's disease, depression, and ADHD. Additionally, its stereochemistry allows for the creation of enantiomerically pure drugs, enhancing efficacy and reducing side effects.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿10,116.00

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(1S,2R)-2-(Methylamino)cyclopentan-1-ol
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This compound is primarily used in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) drugs. Its structure, featuring a cyclopentane ring with hydroxyl and methylamino groups, makes it a valuable intermediate in creating molecules that interact with neurotransmitter systems. It is often utilized in the production of compounds targeting adrenergic and dopaminergic receptors, which are critical in treating conditions like Parkinson's disease, depression,

This compound is primarily used in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) drugs. Its structure, featuring a cyclopentane ring with hydroxyl and methylamino groups, makes it a valuable intermediate in creating molecules that interact with neurotransmitter systems. It is often utilized in the production of compounds targeting adrenergic and dopaminergic receptors, which are critical in treating conditions like Parkinson's disease, depression, and ADHD. Additionally, its stereochemistry allows for the creation of enantiomerically pure drugs, enhancing efficacy and reducing side effects.

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