Ethyl 2-hydroxy-6-methylbenzoate

98%

Reagent Code: #182357
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CAS Number 6555-40-4

science Other reagents with same CAS 6555-40-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.2 g/mol
Formula C₁₀H₁₂O₃
thermostat Physical Properties
Melting Point 45°C
Boiling Point 248.6°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs). It serves as a building block in organic reactions due to the presence of both ester and phenolic functional groups, enabling derivatization for drug development. Also employed in the preparation of UV-absorbing compounds for use in sunscreens and protective coatings. Its methyl and hydroxyl substituents allow for selective modification in multi-step synthetic pathways.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿1,240.00
Ethyl 2-hydroxy-6-methylbenzoate
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs). It serves as a building block in organic reactions due to the presence of both ester and phenolic functional groups, enabling derivatization for drug development. Also employed in the preparation of UV-absorbing compounds for use in sunscreens and protective coatings. Its methyl and hydroxyl substituents allow for selective modification in multi-

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs). It serves as a building block in organic reactions due to the presence of both ester and phenolic functional groups, enabling derivatization for drug development. Also employed in the preparation of UV-absorbing compounds for use in sunscreens and protective coatings. Its methyl and hydroxyl substituents allow for selective modification in multi-step synthetic pathways.

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