(3S,4S)-3-Amino-1-chloro-4-methylhexan-2-one hydrochloride

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Reagent Code: #36782
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CAS Number 59079-44-6

science Other reagents with same CAS 59079-44-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.1061 g/mol
Formula C₇H₁₅Cl₂NO
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MDL Number MFCD19443520
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its chiral structure makes it valuable for creating enantiomerically pure drugs, particularly in the development of central nervous system (CNS) agents and other therapeutic compounds. The presence of both amino and chloro groups allows for versatile chemical modifications, enabling the production of derivatives with potential pharmacological activities. It is also utilized in organic synthesis for constructing complex molecular frameworks, contributing to advancements in medicinal chemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,287.00

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(3S,4S)-3-Amino-1-chloro-4-methylhexan-2-one hydrochloride
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Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its chiral structure makes it valuable for creating enantiomerically pure drugs, particularly in the development of central nervous system (CNS) agents and other therapeutic compounds. The presence of both amino and chloro groups allows for versatile chemical modifications, enabling the production of derivatives with potential pharmacological activities. I

Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its chiral structure makes it valuable for creating enantiomerically pure drugs, particularly in the development of central nervous system (CNS) agents and other therapeutic compounds. The presence of both amino and chloro groups allows for versatile chemical modifications, enabling the production of derivatives with potential pharmacological activities. It is also utilized in organic synthesis for constructing complex molecular frameworks, contributing to advancements in medicinal chemistry and drug discovery.

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