Methyl 2,3-dimethylbenzoate

≥95%

Reagent Code: #205777
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CAS Number 15012-36-9

science Other reagents with same CAS 15012-36-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 164.20 g/mol
Formula C₁₀H₁₂O₂
badge Registry Numbers
MDL Number MFCD06203773
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its aromatic ester structure makes it suitable for use in fragrance formulations, contributing to fruity or floral notes in perfumes and flavorings. It also serves as a building block in the preparation of more complex molecules through reactions such as hydrolysis, reduction, or cross-coupling. Due to its methyl substitution pattern, it is valuable in research for studying steric effects in reaction pathways.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿1,300.00
10g
10-20 days ฿2,360.00
25g
10-20 days ฿5,840.00
100g
10-20 days ฿19,920.00
500g
10-20 days ฿75,430.00
Methyl 2,3-dimethylbenzoate
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Used primarily as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its aromatic ester structure makes it suitable for use in fragrance formulations, contributing to fruity or floral notes in perfumes and flavorings. It also serves as a building block in the preparation of more complex molecules through reactions such as hydrolysis, reduction, or cross-coupling. Due to its methyl substitution pattern, it is valuable in research for studying steric

Used primarily as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its aromatic ester structure makes it suitable for use in fragrance formulations, contributing to fruity or floral notes in perfumes and flavorings. It also serves as a building block in the preparation of more complex molecules through reactions such as hydrolysis, reduction, or cross-coupling. Due to its methyl substitution pattern, it is valuable in research for studying steric effects in reaction pathways.

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