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Home  > 2-(2-Aminoethyl)-2,3-dihydro-1h-isoindole-1,3-dione hydrochloride

AB38929

30250-67-0 | 2-(2-Aminoethyl)-2,3-dihydro-1h-isoindole-1,3-dione hydrochloride

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $49.00 $35.00 -   +
1g 97% in stock $59.00 $42.00 -   +
5g 97% in stock $231.00 $162.00 -   +
10g 97% in stock $384.00 $269.00 -   +
25g 97% in stock $831.00 $582.00 -   +
100g 97% in stock $2,111.00 $1,478.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB38929
Chemical Name: 2-(2-Aminoethyl)-2,3-dihydro-1h-isoindole-1,3-dione hydrochloride
CAS Number: 30250-67-0
Molecular Formula: C10H11ClN2O2
Molecular Weight: 226.6595
MDL Number: MFCD08272836
SMILES: NCCN1C(=O)c2c(C1=O)cccc2.Cl

 

Computed Properties
Complexity: 241  
Covalently-Bonded Unit Count: 2  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 2  

 

 

Upstream Synthesis Route
  • 2-(2-Aminoethyl)isoindoline-1,3-dione hydrochloride, commonly known as $name$, is a versatile compound used in chemical synthesis processes. This compound serves as a crucial building block in the creation of various organic molecules and pharmaceutical intermediates. Its primary application lies in peptide synthesis, where it can be employed as a key reagent for the formation of peptide bonds. Additionally, $name$ has found utility in the preparation of complex heterocyclic compounds due to its ability to participate in various cycloaddition reactions. Furthermore, its unique structure enables it to act as a chiral auxiliary in asymmetric synthesis, facilitating the production of enantiomerically pure compounds. In summary, the significance of 2-(2-Aminoethyl)isoindoline-1,3-dione hydrochloride in chemical synthesis is evident in its versatility and multiple roles across different synthetic pathways.
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