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AE18743

103067-78-3 | (R)-2-Aminohex-5-enoic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $110.00 $77.00 -   +
250mg 97% in stock $177.00 $124.00 -   +
1g 97% in stock $469.00 $329.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE18743
Chemical Name: (R)-2-Aminohex-5-enoic acid
CAS Number: 103067-78-3
Molecular Formula: C6H11NO2
Molecular Weight: 129.1570
MDL Number: MFCD19204099
SMILES: N[C@@H](C(=O)O)CCC=C

 

Computed Properties
Complexity: 112  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 4  
XLogP3: -1.9  

 

 

Upstream Synthesis Route
  • The (R)-2-Aminohex-5-enoic acid, commonly known as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role in organic chemistry as a key building block for the production of various pharmaceuticals, agrochemicals, and functional materials. In chemical synthesis, (R)-2-Aminohex-5-enoic acid acts as a valuable precursor in the formation of peptide bonds, which are essential for the creation of peptides and proteins. The presence of an amino group and a double bond in its structure allows for diverse transformations and functional group manipulations, enabling the generation of complex molecular structures.Furthermore, (R)-2-Aminohex-5-enoic acid can be utilized in the development of chiral ligands for asymmetric catalysis, facilitating the synthesis of enantiopure compounds with high stereocontrol. Its strategic incorporation in various synthetic routes contributes to the efficient construction of chemical compounds with specific stereochemical properties.Moreover, the unique reactivity of (R)-2-Aminohex-5-enoic acid makes it a valuable intermediate in the synthesis of bioactive molecules, natural products, and specialty chemicals. Its ability to undergo selective transformations under mild reaction conditions enhances the synthetic efficiency and overall yield of target molecules, making it a valuable asset in the chemical synthesis toolbox.
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