(S)-1-chloro-3-((4-chlorobenzylidene)amino)propan-2-ol

99%

Reagent Code: #62363
label
Alias (S)-1-Chloro-3-{[(4-chlorophenyl)methylene]amino}propan-2-ol
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CAS Number 1345879-87-9

science Other reagents with same CAS 1345879-87-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.1 g/mol
Formula C₁₀H₁₁Cl₂NO
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmacologically active compounds. Its structure, featuring both chloro and amino groups, makes it a versatile building block for the development of chiral molecules, which are crucial in the synthesis of certain drugs and agrochemicals. Additionally, it is employed in research settings to study the behavior of chiral compounds and their interactions in biological systems. The compound’s reactivity also allows it to be used in the preparation of ligands for catalysis, particularly in asymmetric synthesis, which is essential for creating enantiomerically pure substances.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,188.00
inventory 5g
10-20 days ฿4,176.00

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(S)-1-chloro-3-((4-chlorobenzylidene)amino)propan-2-ol
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This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmacologically active compounds. Its structure, featuring both chloro and amino groups, makes it a versatile building block for the development of chiral molecules, which are crucial in the synthesis of certain drugs and agrochemicals. Additionally, it is employed in research settings to study the behavior of chiral compounds and their interactions in biological sys

This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmacologically active compounds. Its structure, featuring both chloro and amino groups, makes it a versatile building block for the development of chiral molecules, which are crucial in the synthesis of certain drugs and agrochemicals. Additionally, it is employed in research settings to study the behavior of chiral compounds and their interactions in biological systems. The compound’s reactivity also allows it to be used in the preparation of ligands for catalysis, particularly in asymmetric synthesis, which is essential for creating enantiomerically pure substances.

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