1-(2,6-dimethylphenoxy)propan-2-one

≥95%

Reagent Code: #170094
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CAS Number 53012-41-2

science Other reagents with same CAS 53012-41-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.23 g/mol
Formula C₁₁H₁₄O₂
badge Registry Numbers
MDL Number MFCD00130266
inventory_2 Storage & Handling
Density 1.05 g/cm3
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of local anesthetics and antiarrhythmic drugs. Its structure supports the development of compounds that modulate ion channels in nerve and cardiac tissues. Also employed in the preparation of chiral building blocks for fine chemicals and active pharmaceutical ingredients (APIs). The compound’s reactivity and stability make it suitable for use in multi-step organic syntheses where selective functional group transformations are required.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,180.00
1g
10-20 days ฿4,130.00
5g
10-20 days ฿12,230.00
500mg
10-20 days ฿2,410.00

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1-(2,6-dimethylphenoxy)propan-2-one
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of local anesthetics and antiarrhythmic drugs. Its structure supports the development of compounds that modulate ion channels in nerve and cardiac tissues. Also employed in the preparation of chiral building blocks for fine chemicals and active pharmaceutical ingredients (APIs). The compound’s reactivity and stability make it suitable for use in multi-step organic syntheses where selective functional group transfo

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of local anesthetics and antiarrhythmic drugs. Its structure supports the development of compounds that modulate ion channels in nerve and cardiac tissues. Also employed in the preparation of chiral building blocks for fine chemicals and active pharmaceutical ingredients (APIs). The compound’s reactivity and stability make it suitable for use in multi-step organic syntheses where selective functional group transformations are required.

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