Methyl 4-chloro-3-hydroxythiophene-2-carboxylate

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Reagent Code: #47158
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CAS Number 65449-59-4

science Other reagents with same CAS 65449-59-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 192.62 g/mol
Formula C₆H₅ClO₃S
badge Registry Numbers
MDL Number MFCD15071696
thermostat Physical Properties
Boiling Point 251.8°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.514g/cm3
Storage 2-8°C, dry and sealed away from light

description Product Description

This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of various pharmaceuticals and agrochemicals. Its unique structure, featuring both chloro and hydroxyl groups on a thiophene ring, makes it valuable for constructing complex molecules, particularly in the synthesis of biologically active compounds. It is often employed in the production of herbicides and fungicides, where its thiophene core contributes to the efficacy of the final product. Additionally, it serves as a building block in medicinal chemistry for designing drugs targeting specific enzymes or receptors, particularly in the development of anti-inflammatory and antimicrobial agents. Its ester functional group allows for further chemical modifications, enabling the creation of diverse derivatives with tailored properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,285.00

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Methyl 4-chloro-3-hydroxythiophene-2-carboxylate
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This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of various pharmaceuticals and agrochemicals. Its unique structure, featuring both chloro and hydroxyl groups on a thiophene ring, makes it valuable for constructing complex molecules, particularly in the synthesis of biologically active compounds. It is often employed in the production of herbicides and fungicides, where its thiophene core contributes to the efficacy of the final product. Additionall

This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of various pharmaceuticals and agrochemicals. Its unique structure, featuring both chloro and hydroxyl groups on a thiophene ring, makes it valuable for constructing complex molecules, particularly in the synthesis of biologically active compounds. It is often employed in the production of herbicides and fungicides, where its thiophene core contributes to the efficacy of the final product. Additionally, it serves as a building block in medicinal chemistry for designing drugs targeting specific enzymes or receptors, particularly in the development of anti-inflammatory and antimicrobial agents. Its ester functional group allows for further chemical modifications, enabling the creation of diverse derivatives with tailored properties.

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