4-chloro-N-(4-formylpiperazine-1-carbothioyl)benzamide

≥90%

Reagent Code: #220410
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CAS Number 497060-71-6

science Other reagents with same CAS 497060-71-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 311.79 g/mol
Formula C₁₃H₁₄ClN₃O₂S
badge Registry Numbers
MDL Number MFCD01859602
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceutical agents targeting enzyme inhibition. Its structure supports conjugation with other functional molecules, making it valuable in medicinal chemistry for designing potential anticonvulsant, antimicrobial, or anti-inflammatory agents. The aldehyde group enables Schiff base formation, useful in creating diverse derivatives for structure-activity relationship studies. Also employed in heterocyclic synthesis to build complex nitrogen-sulfur containing rings with potential pharmacological activity.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿7,380.00

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4-chloro-N-(4-formylpiperazine-1-carbothioyl)benzamide
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Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceutical agents targeting enzyme inhibition. Its structure supports conjugation with other functional molecules, making it valuable in medicinal chemistry for designing potential anticonvulsant, antimicrobial, or anti-inflammatory agents. The aldehyde group enables Schiff base formation, useful in creating diverse derivatives for structure-activity relationship studies. Also employed in het

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceutical agents targeting enzyme inhibition. Its structure supports conjugation with other functional molecules, making it valuable in medicinal chemistry for designing potential anticonvulsant, antimicrobial, or anti-inflammatory agents. The aldehyde group enables Schiff base formation, useful in creating diverse derivatives for structure-activity relationship studies. Also employed in heterocyclic synthesis to build complex nitrogen-sulfur containing rings with potential pharmacological activity.

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