3,4,5-Trimethoxybenzoyl Chloride

98%

Reagent Code: #240997
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CAS Number 4521-61-3

science Other reagents with same CAS 4521-61-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.65 g/mol
Formula C₁₀H₁₁ClO₄
badge Registry Numbers
MDL Number MFCD00000675
thermostat Physical Properties
Melting Point 81-84 °C
Boiling Point 185 °C18 mm Hg
inventory_2 Storage & Handling
Density 1,214 g/mL
Storage  2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry. It plays a key role in the preparation of vasodilator drugs such as papaverine, which is used to treat blood vessel spasms and improve blood flow. Its reactivity allows it to form amide and ester derivatives, making it valuable for constructing complex bioactive molecules. Also employed in the synthesis of natural product analogs and in the development of new therapeutic agents where a trimethoxybenzoyl moiety is required. Its acyl chloride group readily participates in coupling reactions, enabling efficient bond formation with amines and alcohols under controlled conditions.

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Size Availability Unit Price Quantity
inventory 100g
10-20 days ฿5,000.00
inventory 500g
10-20 days ฿24,100.00

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3,4,5-Trimethoxybenzoyl Chloride
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Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry. It plays a key role in the preparation of vasodilator drugs such as papaverine, which is used to treat blood vessel spasms and improve blood flow. Its reactivity allows it to form amide and ester derivatives, making it valuable for constructing complex bioactive molecules. Also employed in the synthesis of natural product analogs and in the development of new therapeutic agents where a trimethoxybenzoyl moi

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry. It plays a key role in the preparation of vasodilator drugs such as papaverine, which is used to treat blood vessel spasms and improve blood flow. Its reactivity allows it to form amide and ester derivatives, making it valuable for constructing complex bioactive molecules. Also employed in the synthesis of natural product analogs and in the development of new therapeutic agents where a trimethoxybenzoyl moiety is required. Its acyl chloride group readily participates in coupling reactions, enabling efficient bond formation with amines and alcohols under controlled conditions.

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