3-Azabicyclo[3.1.0]hexane-2-carboxylic acid

≥95%

Reagent Code: #137315
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CAS Number 22255-16-9

science Other reagents with same CAS 22255-16-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 127.14 g/mol
Formula C₆H₉NO₂
badge Registry Numbers
MDL Number MFCD08436672
thermostat Physical Properties
Melting Point 252-256 °C(lit.)
Boiling Point 280.3±23.0 °C
inventory_2 Storage & Handling
Density 1.327±0.06 g/cm3
Storage Room temperature, dry, sealed

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of glycine transporter inhibitors for neurological disorders. Its rigid bicyclic structure enhances binding selectivity in drug candidates targeting cognitive and psychiatric conditions. Also employed in agrochemicals to improve metabolic stability in active ingredients. The compound’s strained ring system enables unique reactivity in catalysis and chiral synthesis.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿2,510.00
inventory 50mg
10-20 days ฿8,030.00

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3-Azabicyclo[3.1.0]hexane-2-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of glycine transporter inhibitors for neurological disorders. Its rigid bicyclic structure enhances binding selectivity in drug candidates targeting cognitive and psychiatric conditions. Also employed in agrochemicals to improve metabolic stability in active ingredients. The compound’s strained ring system enables unique reactivity in catalysis and chiral synthesis.

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of glycine transporter inhibitors for neurological disorders. Its rigid bicyclic structure enhances binding selectivity in drug candidates targeting cognitive and psychiatric conditions. Also employed in agrochemicals to improve metabolic stability in active ingredients. The compound’s strained ring system enables unique reactivity in catalysis and chiral synthesis.

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