Tetrahydrofuran-3-ylamine hydrochloride

95%

Reagent Code: #240035
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CAS Number 204512-94-7

science Other reagents with same CAS 204512-94-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 123.58 g/mol
Formula C₄H₁₀ClNO
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for central nervous system drugs. Its structure serves as a building block in creating compounds with neurological activity, including antidepressants and antipsychotics. Also employed in the preparation of specialty polymers and agrochemicals due to its reactivity and solubility properties. Commonly utilized in research settings for heterocyclic compound development and in the creation of chiral auxiliaries for asymmetric synthesis.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿198.00
inventory 1g
10-20 days ฿456.00
inventory 5g
10-20 days ฿2,900.00
Tetrahydrofuran-3-ylamine hydrochloride
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for central nervous system drugs. Its structure serves as a building block in creating compounds with neurological activity, including antidepressants and antipsychotics. Also employed in the preparation of specialty polymers and agrochemicals due to its reactivity and solubility properties. Commonly utilized in research settings for heterocyclic compound development and in the creation of c

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for central nervous system drugs. Its structure serves as a building block in creating compounds with neurological activity, including antidepressants and antipsychotics. Also employed in the preparation of specialty polymers and agrochemicals due to its reactivity and solubility properties. Commonly utilized in research settings for heterocyclic compound development and in the creation of chiral auxiliaries for asymmetric synthesis.

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