logo
Home  > 1-Amino-2-propanol

AB74919

78-96-6 | 1-Amino-2-propanol

Packsize Purity Availability Price Discounted Price    Quantity
5g 92% in stock $25.00 $17.00 -   +
25g 92% in stock $28.00 $20.00 -   +
500g 92% in stock $37.00 $26.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB74919
Chemical Name: 1-Amino-2-propanol
CAS Number: 78-96-6
Molecular Formula: C3H9NO
Molecular Weight: 75.1097
MDL Number: MFCD00008139
SMILES: CC(CN)O
NSC Number: 3188

 

Computed Properties
Complexity: 22.9  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 5  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 1  
Undefined Atom Stereocenter Count: 1  
XLogP3: -1  

 

 

Upstream Synthesis Route
  • The versatile compound 1-Aminopropan-2-ol plays a crucial role in chemical synthesis as a valuable building block for various applications. Its primary function lies in its ability to serve as a key intermediate in the synthesis of numerous important chemicals and pharmaceuticals. Through strategic manipulation of its chemical structure, 1-Aminopropan-2-ol can be transformed into a wide array of derivatives, each with unique properties and functions.In organic synthesis, 1-Aminopropan-2-ol is frequently employed as a precursor for the preparation of complex molecules such as pharmaceuticals, agrochemicals, and functional materials. Its versatility stems from the presence of both amine and alcohol functional groups, which enable it to participate in a variety of organic reactions. By undergoing processes such as alkylation, acylation, or oxidation, 1-Aminopropan-2-ol can be modified to introduce specific functional groups or alter its chemical properties as needed for a particular synthetic pathway.Furthermore, 1-Aminopropan-2-ol serves as a valuable chiral building block in asymmetric synthesis, allowing chemists to access enantiomerically pure compounds with high selectivity. By utilizing chiral auxiliaries or catalysts, the stereochemistry of 1-Aminopropan-2-ol can be leveraged to control the stereochemical outcome of subsequent reactions, leading to the selective formation of desired chiral products.Overall, 1-Aminopropan-2-ol's significance in chemical synthesis lies in its adaptability and utility as a key intermediate for the construction of diverse organic molecules. Its versatility and functional groups make it a valuable resource for designing and accessing complex molecular structures with high efficiency and precision.
FEATURED PRODUCTS