Methyl 4-amino-3-(tert-butyl)benzoate hydrochloride

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Reagent Code: #119016
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CAS Number 2044702-89-6

science Other reagents with same CAS 2044702-89-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.73 g/mol
Formula C₁₂H₁₈ClNO₂
badge Registry Numbers
MDL Number MFCD30609550
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound, Methyl 4-amino-3-(tert-butyl)benzoate hydrochloride, serves as a key intermediate in pharmaceutical research and development for the synthesis of active pharmaceutical ingredients (APIs). It is particularly utilized in creating drugs targeting anti-inflammatory effects, pain relief, and potential anti-cancer therapies, leveraging its amino and ester functional groups for structural modifications that improve efficacy and specificity. These modifications enable inhibition of enzymes or biochemical pathways involved in disease processes, such as inflammation or cancer cell growth. Additionally, it is applied in organic synthesis to build complex molecules and explore reaction mechanisms.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,934.00
inventory 100mg
10-20 days ฿1,467.00

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Methyl 4-amino-3-(tert-butyl)benzoate hydrochloride
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This compound, Methyl 4-amino-3-(tert-butyl)benzoate hydrochloride, serves as a key intermediate in pharmaceutical research and development for the synthesis of active pharmaceutical ingredients (APIs). It is particularly utilized in creating drugs targeting anti-inflammatory effects, pain relief, and potential anti-cancer therapies, leveraging its amino and ester functional groups for structural modifications that improve efficacy and specificity. These modifications enable inhibition of enzymes or bioc

This compound, Methyl 4-amino-3-(tert-butyl)benzoate hydrochloride, serves as a key intermediate in pharmaceutical research and development for the synthesis of active pharmaceutical ingredients (APIs). It is particularly utilized in creating drugs targeting anti-inflammatory effects, pain relief, and potential anti-cancer therapies, leveraging its amino and ester functional groups for structural modifications that improve efficacy and specificity. These modifications enable inhibition of enzymes or biochemical pathways involved in disease processes, such as inflammation or cancer cell growth. Additionally, it is applied in organic synthesis to build complex molecules and explore reaction mechanisms.

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