4-Amino-3-chloro-5-hydroxybenzoic acid

98%

Reagent Code: #130162
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CAS Number 202195-65-1

science Other reagents with same CAS 202195-65-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.58 g/mol
Formula C₇H₆ClNO₃
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MDL Number MFCD20640484
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of certain antibiotics and antimicrobial agents, particularly in the production of chloramphenicol analogs. It plays a role in constructing complex aromatic frameworks due to the presence of multiple functional groups (amino, chloro, hydroxy, and carboxylic acid), which allow for selective chemical modifications. Commonly employed in pharmaceutical research for developing bioactive molecules and in the preparation of specialty chemicals requiring regioselective substitution patterns on the benzene ring.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿7,520.00
250mg
10-20 days ฿12,710.00
1g
10-20 days ฿34,150.00
4-Amino-3-chloro-5-hydroxybenzoic acid
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Used as an intermediate in the synthesis of certain antibiotics and antimicrobial agents, particularly in the production of chloramphenicol analogs. It plays a role in constructing complex aromatic frameworks due to the presence of multiple functional groups (amino, chloro, hydroxy, and carboxylic acid), which allow for selective chemical modifications. Commonly employed in pharmaceutical research for developing bioactive molecules and in the preparation of specialty chemicals requiring regioselective su

Used as an intermediate in the synthesis of certain antibiotics and antimicrobial agents, particularly in the production of chloramphenicol analogs. It plays a role in constructing complex aromatic frameworks due to the presence of multiple functional groups (amino, chloro, hydroxy, and carboxylic acid), which allow for selective chemical modifications. Commonly employed in pharmaceutical research for developing bioactive molecules and in the preparation of specialty chemicals requiring regioselective substitution patterns on the benzene ring.

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