2-Amino-2,3-dimethylbutyramide

95%

Reagent Code: #135614
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CAS Number 40963-14-2

science Other reagents with same CAS 40963-14-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 130.19 g/mol
Formula C₆H₁₄N₂O
thermostat Physical Properties
Melting Point 74.5-76°C
Boiling Point 242.6°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of active ingredients for central nervous system (CNS) drugs. It serves as a chiral building block in organic synthesis, enabling the production of structurally complex molecules with high stereoselectivity. Its amide and amino functional groups allow for peptide coupling and derivatization, making it valuable in medicinal chemistry for designing bioactive compounds. Also employed in the preparation of agrochemicals and specialty polymers due to its structural stability and reactivity profile.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿156.00
inventory 10g
10-20 days ฿500.00
inventory 50g
10-20 days ฿1,550.00
inventory 250g
10-20 days ฿5,940.00
inventory 1kg
10-20 days ฿18,730.00

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2-Amino-2,3-dimethylbutyramide
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of active ingredients for central nervous system (CNS) drugs. It serves as a chiral building block in organic synthesis, enabling the production of structurally complex molecules with high stereoselectivity. Its amide and amino functional groups allow for peptide coupling and derivatization, making it valuable in medicinal chemistry for designing bioactive compounds. Also employed in the preparation of agrochemicals an

Used in the synthesis of pharmaceutical intermediates, particularly in the development of active ingredients for central nervous system (CNS) drugs. It serves as a chiral building block in organic synthesis, enabling the production of structurally complex molecules with high stereoselectivity. Its amide and amino functional groups allow for peptide coupling and derivatization, making it valuable in medicinal chemistry for designing bioactive compounds. Also employed in the preparation of agrochemicals and specialty polymers due to its structural stability and reactivity profile.

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