Methyl 2-((4-hydroxyphenyl)amino)acetate hydrochloride

95%

Reagent Code: #207298
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CAS Number 113210-35-8

science Other reagents with same CAS 113210-35-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.65 g/mol
Formula C₉H₁₂ClNO₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in pharmaceutical synthesis as an intermediate for developing bioactive compounds, particularly in the production of kinase inhibitors and anti-inflammatory agents. It serves as a building block in the preparation of tyrosine-derived analogs with potential anticancer properties. Also applied in research settings for structure-activity relationship studies due to its phenolic and ester functionalities. The hydrochloride salt form enhances solubility and stability in aqueous reaction environments.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿700.00
inventory 250mg
10-20 days ฿890.00
inventory 1g
10-20 days ฿2,460.00
inventory 5g
10-20 days ฿5,533.00

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Methyl 2-((4-hydroxyphenyl)amino)acetate hydrochloride
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Used in pharmaceutical synthesis as an intermediate for developing bioactive compounds, particularly in the production of kinase inhibitors and anti-inflammatory agents. It serves as a building block in the preparation of tyrosine-derived analogs with potential anticancer properties. Also applied in research settings for structure-activity relationship studies due to its phenolic and ester functionalities. The hydrochloride salt form enhances solubility and stability in aqueous reaction environments.

Used in pharmaceutical synthesis as an intermediate for developing bioactive compounds, particularly in the production of kinase inhibitors and anti-inflammatory agents. It serves as a building block in the preparation of tyrosine-derived analogs with potential anticancer properties. Also applied in research settings for structure-activity relationship studies due to its phenolic and ester functionalities. The hydrochloride salt form enhances solubility and stability in aqueous reaction environments.

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