METHYL N-[2-(4-HYDROXYPHENYL)ETHYL]CARBAMATE

≥99%

Reagent Code: #203870
label
Alias Methyl 4-hydroxyphenylethylaminomethyl ester; Methyl [2-(4-hydroxyphenyl)ethyl]carbamate
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CAS Number 62372-08-1

science Other reagents with same CAS 62372-08-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 195.22 g/mol
Formula C₁₀H₁₃NO₃
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting muscle relaxants and neuroactive compounds. Its structure supports modification for enhancing blood-brain barrier penetration, making it valuable in designing drugs targeting the central nervous system. Also explored in prodrug strategies due to the presence of the phenolic hydroxyl group, allowing for esterification or conjugation to improve pharmacokinetic properties.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿990.00
250mg
10-20 days ฿2,340.00
1g
10-20 days ฿7,740.00
25g
10-20 days ฿77,660.00
100g
10-20 days ฿282,690.00
5g
10-20 days ฿25,890.00
METHYL N-[2-(4-HYDROXYPHENYL)ETHYL]CARBAMATE
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting muscle relaxants and neuroactive compounds. Its structure supports modification for enhancing blood-brain barrier penetration, making it valuable in designing drugs targeting the central nervous system. Also explored in prodrug strategies due to the presence of the phenolic hydroxyl group, allowing for esterification or conjugation to improve pharmacokinetic properties.

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting muscle relaxants and neuroactive compounds. Its structure supports modification for enhancing blood-brain barrier penetration, making it valuable in designing drugs targeting the central nervous system. Also explored in prodrug strategies due to the presence of the phenolic hydroxyl group, allowing for esterification or conjugation to improve pharmacokinetic properties.

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