3-Chloro-N-(3-chlorophenyl)propanamide

95%

Reagent Code: #162587
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CAS Number 99585-98-5

science Other reagents with same CAS 99585-98-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.08 g/mol
Formula C₉H₉Cl₂NO
badge Registry Numbers
MDL Number MFCD01213638
thermostat Physical Properties
Boiling Point 384.5°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. It serves as a building block for compounds with potential anticonvulsant and neuroprotective properties. Also employed in research settings to design novel bioactive molecules due to its halogenated aromatic and amide functionalities, which enhance binding selectivity in drug-receptor interactions.

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Test Parameter Specification
Appearance white solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,830.00
inventory 5g
10-20 days ฿13,670.00
inventory 1g
10-20 days ฿1,704.00

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3-Chloro-N-(3-chlorophenyl)propanamide
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. It serves as a building block for compounds with potential anticonvulsant and neuroprotective properties. Also employed in research settings to design novel bioactive molecules due to its halogenated aromatic and amide functionalities, which enhance binding selectivity in drug-receptor interactions.

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. It serves as a building block for compounds with potential anticonvulsant and neuroprotective properties. Also employed in research settings to design novel bioactive molecules due to its halogenated aromatic and amide functionalities, which enhance binding selectivity in drug-receptor interactions.

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