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AE23298

1209287-84-2 | 1-Methylpyrrolidin-3-amine dihydrochloride

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $16.00 $12.00 -   +
1g 97% in stock $41.00 $29.00 -   +
5g 97% in stock $148.00 $104.00 -   +
10g 97% in stock $296.00 $208.00 -   +
25g 97% in stock $740.00 $518.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AE23298
Chemical Name: 1-Methylpyrrolidin-3-amine dihydrochloride
CAS Number: 1209287-84-2
Molecular Formula: C5H14Cl2N2
Molecular Weight: 173.0841
MDL Number: MFCD13195986
SMILES: CN1CCC(C1)N.Cl.Cl

 

Computed Properties
Complexity: 63.1  
Covalently-Bonded Unit Count: 3  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 3  
Undefined Atom Stereocenter Count: 1  

 

 

Upstream Synthesis Route
  • 1-Methylpyrrolidin-3-amine dihydrochloride, also known as $name$, is a key reagent used in chemical synthesis due to its versatile applications. This compound is commonly employed as a powerful nucleophilic organocatalyst in various reactions, particularly in the field of organic and medicinal chemistry. Its unique structure and reactivity make it an ideal choice for facilitating a wide range of transformations.In chemical synthesis, 1-Methylpyrrolidin-3-amine dihydrochloride can serve as a catalyst in asymmetric transformations, promoting the formation of chiral compounds with high enantioselectivity. It can also act as a Lewis base in reactions involving electrophilic substrates, enabling the formation of complex molecular structures. Furthermore, this reagent is valuable in promoting cyclization reactions, ring-opening processes, and other key steps in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals.Overall, the use of 1-Methylpyrrolidin-3-amine dihydrochloride provides chemists with a powerful tool for streamlining synthetic pathways, enhancing reaction efficiency, and accessing a diverse array of chemical scaffolds. Its versatility and efficacy make it an indispensable component in the toolkit of synthetic chemists striving to develop novel molecules with unique properties.
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