3-(2-Aminoethyl)phenol

95%

Reagent Code: #137733
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Alias 38449-59-1
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CAS Number 588-05-6

science Other reagents with same CAS 588-05-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 137.18 g/mol
Formula C₈H₁₁NO
badge Registry Numbers
MDL Number MFCD06654561
thermostat Physical Properties
Melting Point 140 °C
Boiling Point 275.5±15.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.103±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of central nervous system agents and antidepressants. It serves as a building block for compounds with neuroactive properties due to its structural similarity to neurotransmitters. Also employed in the development of specialty polymers and resins where enhanced reactivity and cross-linking are required. Its amine and phenolic functional groups allow for versatile chemical modifications, making it valuable in research and development of bioactive molecules and functional materials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,300.00
inventory 250mg
10-20 days ฿9,900.00

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3-(2-Aminoethyl)phenol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of central nervous system agents and antidepressants. It serves as a building block for compounds with neuroactive properties due to its structural similarity to neurotransmitters. Also employed in the development of specialty polymers and resins where enhanced reactivity and cross-linking are required. Its amine and phenolic functional groups allow for versatile chemical modifications, making it valuable in re

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of central nervous system agents and antidepressants. It serves as a building block for compounds with neuroactive properties due to its structural similarity to neurotransmitters. Also employed in the development of specialty polymers and resins where enhanced reactivity and cross-linking are required. Its amine and phenolic functional groups allow for versatile chemical modifications, making it valuable in research and development of bioactive molecules and functional materials.

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