Methyl3-amino-4-chloro-1-benzothiophene-2-carboxylate

98%

Reagent Code: #214161
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CAS Number 35212-86-3

science Other reagents with same CAS 35212-86-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.69 g/mol
Formula C₁₀H₈ClNO₂S
badge Registry Numbers
MDL Number MFCD01566406
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) active compounds. Its structure supports the construction of heterocyclic frameworks found in bioactive molecules. Commonly employed in medicinal chemistry for derivatization to enhance pharmacokinetic properties. Also utilized in research settings for the preparation of benzothiophene-based compounds with potential anticonvulsant, anti-inflammatory, or anticancer activities.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿9,520.00
5g
10-20 days ฿44,550.00
Methyl3-amino-4-chloro-1-benzothiophene-2-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) active compounds. Its structure supports the construction of heterocyclic frameworks found in bioactive molecules. Commonly employed in medicinal chemistry for derivatization to enhance pharmacokinetic properties. Also utilized in research settings for the preparation of benzothiophene-based compounds with potential

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) active compounds. Its structure supports the construction of heterocyclic frameworks found in bioactive molecules. Commonly employed in medicinal chemistry for derivatization to enhance pharmacokinetic properties. Also utilized in research settings for the preparation of benzothiophene-based compounds with potential anticonvulsant, anti-inflammatory, or anticancer activities.

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