5-Chloro-3-nitro-1H-indole

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Reagent Code: #48416
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CAS Number 213542-01-9

science Other reagents with same CAS 213542-01-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.5905 g/mol
Formula C₈H₅ClN₂O₂
badge Registry Numbers
MDL Number MFCD10574688
thermostat Physical Properties
Melting Point 218-220℃
Boiling Point 396℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.564 g/cm3
Storage 2-8°C, dry, airtight

description Product Description

Used primarily in organic synthesis, it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure is valuable in the development of compounds with potential biological activity, particularly in the creation of indole-based drugs. It is also employed in research settings to study chemical reactions involving nitro and chloro substituents on indole rings, aiding in the discovery of new therapeutic agents. Additionally, it finds application in the synthesis of dyes and pigments due to its aromatic properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,552.00
inventory 1g
10-20 days ฿23,292.00

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5-Chloro-3-nitro-1H-indole
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Used primarily in organic synthesis, it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure is valuable in the development of compounds with potential biological activity, particularly in the creation of indole-based drugs. It is also employed in research settings to study chemical reactions involving nitro and chloro substituents on indole rings, aiding in the discovery of new therapeutic agents. Additionally, it finds application in the synthesis o

Used primarily in organic synthesis, it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure is valuable in the development of compounds with potential biological activity, particularly in the creation of indole-based drugs. It is also employed in research settings to study chemical reactions involving nitro and chloro substituents on indole rings, aiding in the discovery of new therapeutic agents. Additionally, it finds application in the synthesis of dyes and pigments due to its aromatic properties.

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