3-Chloro-N-(3-hydroxyphenyl)propanamide

95%

Reagent Code: #162785
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CAS Number 50297-40-0

science Other reagents with same CAS 50297-40-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.63 g/mol
Formula C₉H₁₀ClNO₂
badge Registry Numbers
MDL Number MFCD02812236
thermostat Physical Properties
Boiling Point 429.2±30.0 °C at 760 mmHg (lit.)
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of pharmaceutical compounds. It serves in the preparation of bioactive molecules due to the presence of both amide and hydroxyl functional groups, which allow for further chemical modifications. Commonly employed in research settings for designing CNS-active agents and anti-inflammatory derivatives. Also utilized in the synthesis of specialty polymers and agrochemicals where chloroalkyl amide scaffolds are required.

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Test Parameter Specification
Appearance Off-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 100mg
10-20 days ฿1,990.00
inventory 1g
10-20 days ฿13,500.00
inventory 5g
10-20 days ฿40,500.00
inventory 25g
10-20 days ฿144,000.00

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3-Chloro-N-(3-hydroxyphenyl)propanamide
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Used as an intermediate in organic synthesis, particularly in the development of pharmaceutical compounds. It serves in the preparation of bioactive molecules due to the presence of both amide and hydroxyl functional groups, which allow for further chemical modifications. Commonly employed in research settings for designing CNS-active agents and anti-inflammatory derivatives. Also utilized in the synthesis of specialty polymers and agrochemicals where chloroalkyl amide scaffolds are required.

Used as an intermediate in organic synthesis, particularly in the development of pharmaceutical compounds. It serves in the preparation of bioactive molecules due to the presence of both amide and hydroxyl functional groups, which allow for further chemical modifications. Commonly employed in research settings for designing CNS-active agents and anti-inflammatory derivatives. Also utilized in the synthesis of specialty polymers and agrochemicals where chloroalkyl amide scaffolds are required.

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