Ethyl [1,1'-biphenyl]-4-carboxylate

97%

Reagent Code: #185326
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CAS Number 6301-56-0

science Other reagents with same CAS 6301-56-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.28 g/mol
Formula C₁₅H₁₄O₂
badge Registry Numbers
MDL Number MFCD00297796
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used primarily as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its biphenyl core structure makes it valuable in the development of liquid crystal materials for display technologies. It also serves as a building block in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs) and related compounds due to the presence of the ester and aromatic functionalities. Additionally, it finds use in research settings for constructing more complex molecules through cross-coupling reactions and functional group transformations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿7,090.00
inventory 25g
10-20 days ฿24,780.00
inventory 100g
10-20 days ฿92,810.00
Ethyl [1,1'-biphenyl]-4-carboxylate
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Used primarily as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its biphenyl core structure makes it valuable in the development of liquid crystal materials for display technologies. It also serves as a building block in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs) and related compounds due to the presence of the ester and aromatic functionalities. Additionally, it finds use in research settings for constructing more complex

Used primarily as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its biphenyl core structure makes it valuable in the development of liquid crystal materials for display technologies. It also serves as a building block in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs) and related compounds due to the presence of the ester and aromatic functionalities. Additionally, it finds use in research settings for constructing more complex molecules through cross-coupling reactions and functional group transformations.

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