(S)-()-Tetrahydrofurfurylamine

98%

Reagent Code: #234611
label
Alias (S)-(+)-tetrahydrofurethaneamine; (S)-(+)-tetrahydrofuranmethylamine
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CAS Number 7175-81-7

science Other reagents with same CAS 7175-81-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 101.15 g/mol
Formula C₅H₁₁NO
badge Registry Numbers
MDL Number MFCD00085303
thermostat Physical Properties
Boiling Point 156.0±13.0 °C at 760 mmHg
inventory_2 Storage & Handling
Density 0.98 g/mL at 25 °C(lit.)
Storage Room temperature, flammable area

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its amine functionality and chiral center make it valuable in asymmetric synthesis and catalysis. Commonly employed in the preparation of neuroactive compounds, agrochemicals, and specialty polymers. Also serves as a precursor in the manufacture of certain antihypertensive and antiviral drugs. Its furan ring structure allows for further functionalization, enabling diverse chemical transformations in medicinal chemistry research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿174.00
inventory 1g
10-20 days ฿940.00
inventory 5g
10-20 days ฿4,640.00
inventory 25g
10-20 days ฿20,550.00
(S)-()-Tetrahydrofurfurylamine
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its amine functionality and chiral center make it valuable in asymmetric synthesis and catalysis. Commonly employed in the preparation of neuroactive compounds, agrochemicals, and specialty polymers. Also serves as a precursor in the manufacture of certain antihypertensive and antiviral drugs. Its furan ring structure allows for further functionalization, enabling diverse chemical transformations in medicinal chemistry research.
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