1-Phenylethane-1,2-diamine dihydrochloride

≥95%

Reagent Code: #226349
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CAS Number 16635-94-2

science Other reagents with same CAS 16635-94-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 209.12 g/mol
Formula C₈H₁₄Cl₂N₂
badge Registry Numbers
MDL Number MFCD01726798
inventory_2 Storage & Handling
Storage Store in an inert gas at room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its diamine structure allows for coordination with metal ions, making it useful in asymmetric catalysis, particularly in the development of chiral ligands for enantioselective reactions. Commonly employed in the preparation of intermediates for central nervous system agents and other fine chemicals. Also finds use in the research of novel organic transformations due to its stereochemical stability and reactivity profile.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,960.00
250mg
10-20 days ฿6,220.00
1g
10-20 days ฿24,440.00
1-Phenylethane-1,2-diamine dihydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its diamine structure allows for coordination with metal ions, making it useful in asymmetric catalysis, particularly in the development of chiral ligands for enantioselective reactions. Commonly employed in the preparation of intermediates for central nervous system agents and other fine chemicals. Also finds use in the research of novel organic transformations due to its stereochemical stability and r

Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its diamine structure allows for coordination with metal ions, making it useful in asymmetric catalysis, particularly in the development of chiral ligands for enantioselective reactions. Commonly employed in the preparation of intermediates for central nervous system agents and other fine chemicals. Also finds use in the research of novel organic transformations due to its stereochemical stability and reactivity profile.

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