2-[(2-chloroacetyl)amino]benzenecarboxylic acid

98%(HPLC)

Reagent Code: #157447
label
Alias 2-[(2-chloroacetyl)amine]benzene carboxylic acid
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CAS Number 14422-49-2

science Other reagents with same CAS 14422-49-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.62 g/mol
Formula C₉H₈ClNO₃
badge Registry Numbers
MDL Number MFCD00029924
thermostat Physical Properties
Melting Point 196-197 °C
Boiling Point 452.7±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.458±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of anthranilic acid derivatives, which are important in the production of dyes, pharmaceuticals, and agrochemicals. It participates in the preparation of heterocyclic compounds due to the presence of both amide and aromatic carboxylic acid functionalities. Its chloroacetyl group allows for further nucleophilic substitution reactions, making it valuable in organic synthesis for building more complex molecules. Commonly employed in the development of active pharmaceutical ingredients where substituted benzamides are required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,200.00
inventory 1g
10-20 days ฿11,980.00
inventory 5g
10-20 days ฿46,800.00

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2-[(2-chloroacetyl)amino]benzenecarboxylic acid
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Used as an intermediate in the synthesis of anthranilic acid derivatives, which are important in the production of dyes, pharmaceuticals, and agrochemicals. It participates in the preparation of heterocyclic compounds due to the presence of both amide and aromatic carboxylic acid functionalities. Its chloroacetyl group allows for further nucleophilic substitution reactions, making it valuable in organic synthesis for building more complex molecules. Commonly employed in the development of active pharmace

Used as an intermediate in the synthesis of anthranilic acid derivatives, which are important in the production of dyes, pharmaceuticals, and agrochemicals. It participates in the preparation of heterocyclic compounds due to the presence of both amide and aromatic carboxylic acid functionalities. Its chloroacetyl group allows for further nucleophilic substitution reactions, making it valuable in organic synthesis for building more complex molecules. Commonly employed in the development of active pharmaceutical ingredients where substituted benzamides are required.

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