(1R,2S)-rel-Cyclopropane-1,2-diamine dihydrochloride

97%

Reagent Code: #228734
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CAS Number 63466-89-7

science Other reagents with same CAS 63466-89-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 145.03 g/mol
Formula C₃H₁₀Cl₂N₂
badge Registry Numbers
MDL Number MFCD12963693
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral building block in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its rigid cyclopropane backbone and two amine groups make it valuable for constructing stereochemically defined molecules, such as protease inhibitors and receptor modulators. Commonly employed in asymmetric synthesis and catalysis, it serves as a ligand precursor or intermediate in the preparation of chiral amines and amino alcohols. Also utilized in the synthesis of agrochemicals and specialty chemicals where stereochemistry plays a critical role in biological activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,550.00
inventory 500mg
10-20 days ฿30,810.00
(1R,2S)-rel-Cyclopropane-1,2-diamine dihydrochloride
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Used as a chiral building block in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its rigid cyclopropane backbone and two amine groups make it valuable for constructing stereochemically defined molecules, such as protease inhibitors and receptor modulators. Commonly employed in asymmetric synthesis and catalysis, it serves as a ligand precursor or intermediate in the preparation of chiral amines and amino alcohols. Al
Used as a chiral building block in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its rigid cyclopropane backbone and two amine groups make it valuable for constructing stereochemically defined molecules, such as protease inhibitors and receptor modulators. Commonly employed in asymmetric synthesis and catalysis, it serves as a ligand precursor or intermediate in the preparation of chiral amines and amino alcohols. Also utilized in the synthesis of agrochemicals and specialty chemicals where stereochemistry plays a critical role in biological activity.
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