Methyl 4-amino-5-chlorothiophene-2-carboxylate

97%

Reagent Code: #207316
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CAS Number 89499-44-5

science Other reagents with same CAS 89499-44-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.64 g/mol
Formula C₆H₆ClNO₂S
thermostat Physical Properties
Melting Point 84-87°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antipsychotic and antihypertensive drugs. It serves as a building block for heterocyclic compounds due to the presence of both amino and ester functional groups, enabling coupling reactions and ring formation. Commonly employed in the preparation of thiophene-based bioactive molecules, including kinase inhibitors and receptor antagonists. Its chloro and amino substituents allow for selective modifications, making it valuable in medicinal chemistry for structure-activity relationship studies. Also utilized in agrochemical research for designing new pesticides with improved efficacy and selectivity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿2,430.00
1g
10-20 days ฿5,380.00
Methyl 4-amino-5-chlorothiophene-2-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antipsychotic and antihypertensive drugs. It serves as a building block for heterocyclic compounds due to the presence of both amino and ester functional groups, enabling coupling reactions and ring formation. Commonly employed in the preparation of thiophene-based bioactive molecules, including kinase inhibitors and receptor antagonists. Its chloro and amino substituents allow for selective modifications,

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antipsychotic and antihypertensive drugs. It serves as a building block for heterocyclic compounds due to the presence of both amino and ester functional groups, enabling coupling reactions and ring formation. Commonly employed in the preparation of thiophene-based bioactive molecules, including kinase inhibitors and receptor antagonists. Its chloro and amino substituents allow for selective modifications, making it valuable in medicinal chemistry for structure-activity relationship studies. Also utilized in agrochemical research for designing new pesticides with improved efficacy and selectivity.

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