(2-Chloro-3-iodophenyl)methanamine

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Reagent Code: #36382
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CAS Number 1261861-09-9

science Other reagents with same CAS 1261861-09-9

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scatter_plot Molecular Information
Weight 267.50 g/mol
Formula C₇H₇ClIN
badge Registry Numbers
MDL Number MFCD18393357
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

(2-Chloro-3-iodophenyl)methanamine is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive compounds, particularly in the synthesis of molecules with potential therapeutic applications. Its structure, featuring both chloro and iodo substituents, makes it a versatile building block for constructing complex chemical entities. This compound is often employed in the preparation of ligands for metal-catalyzed reactions, as well as in the design of drugs targeting neurological disorders or other medical conditions. Its halogenated aromatic ring also makes it useful in the study of structure-activity relationships in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿18,063.00
inventory 100mg
10-20 days ฿9,027.00

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(2-Chloro-3-iodophenyl)methanamine
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(2-Chloro-3-iodophenyl)methanamine is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive compounds, particularly in the synthesis of molecules with potential therapeutic applications. Its structure, featuring both chloro and iodo substituents, makes it a versatile building block for constructing complex chemical entities. This compound is often employed in the preparation of ligands for metal-catalyzed reactions, as wel

(2-Chloro-3-iodophenyl)methanamine is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive compounds, particularly in the synthesis of molecules with potential therapeutic applications. Its structure, featuring both chloro and iodo substituents, makes it a versatile building block for constructing complex chemical entities. This compound is often employed in the preparation of ligands for metal-catalyzed reactions, as well as in the design of drugs targeting neurological disorders or other medical conditions. Its halogenated aromatic ring also makes it useful in the study of structure-activity relationships in medicinal chemistry.

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