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Home  > 1,3-Propanediol, 2-(2-aminoethyl)-

AD78932

105595-59-3 | 1,3-Propanediol, 2-(2-aminoethyl)-

Packsize Purity Availability Price Discounted Price    Quantity
50mg 95% 3 weeks $1,226.00 $858.00 -   +
100mg 95% 3 weeks $1,717.00 $1,202.00 -   +
250mg 95% 3 weeks $2,362.00 $1,654.00 -   +
500mg 95% 3 weeks $3,588.00 $2,512.00 -   +
1g 95% 3 weeks $4,535.00 $3,175.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AD78932
Chemical Name: 1,3-Propanediol, 2-(2-aminoethyl)-
CAS Number: 105595-59-3
Molecular Formula: C5H13NO2
Molecular Weight: 119.1622
MDL Number: MFCD09036507
SMILES: NCCC(CO)CO

 

Upstream Synthesis Route
  • 1,3-Propanediol, 2-(2-aminoethyl)-, also known as ethyltrimethylenediamine, is a versatile chemical compound widely used in various chemical synthesis applications. This compound is commonly utilized as a building block in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique chemical structure makes it an important intermediate in the synthesis of numerous complex organic compounds.In chemical synthesis, 1,3-Propanediol, 2-(2-aminoethyl)- serves as a key starting material for the preparation of various heterocyclic compounds, such as pyrrolidines, piperidines, and pyrazines. It can undergo different types of reactions, including acylation, alkylation, and cyclization, to yield a wide range of organic products with diverse functionalities. Additionally, the presence of the aminoethyl group in the molecule enables the formation of amine derivatives through further functionalization reactions.Furthermore, 1,3-Propanediol, 2-(2-aminoethyl)- is commonly employed in the synthesis of chiral compounds due to its stereochemical properties. By incorporating this compound into asymmetric synthesis strategies, chemists can access enantiomerically pure molecules that have important applications in the pharmaceutical and agrochemical industries. Its versatility in chemical transformations and compatibility with various synthetic methodologies make it a valuable tool for organic chemists seeking to access structurally diverse and complex molecules.
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