Methyl 5-(2-hydroxyethyl)thiophene-2-carboxylate

≥95%

Reagent Code: #209238
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CAS Number 160744-13-8

science Other reagents with same CAS 160744-13-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.23 g/mol
Formula C₈H₁₀O₃S
badge Registry Numbers
MDL Number MFCD12911672
inventory_2 Storage & Handling
Density 1.266g/cm3
Storage 2-8°C, dry and sealed from light

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders. Its structure allows for functionalization that can enhance binding affinity to specific receptors. Also employed in the preparation of biologically active molecules due to the presence of both ester and hydroxyethyl groups, enabling diverse chemical modifications. Additionally, it serves as a building block in the creation of specialty organic compounds for research in medicinal chemistry.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿3,430.00
250mg
10-20 days ฿5,220.00
1g
10-20 days ฿13,480.00
5g
10-20 days ฿47,010.00
Methyl 5-(2-hydroxyethyl)thiophene-2-carboxylate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders. Its structure allows for functionalization that can enhance binding affinity to specific receptors. Also employed in the preparation of biologically active molecules due to the presence of both ester and hydroxyethyl groups, enabling diverse chemical modifications. Additionally, it serves as a building block in the creation of specialty organic compounds for re

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders. Its structure allows for functionalization that can enhance binding affinity to specific receptors. Also employed in the preparation of biologically active molecules due to the presence of both ester and hydroxyethyl groups, enabling diverse chemical modifications. Additionally, it serves as a building block in the creation of specialty organic compounds for research in medicinal chemistry.

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