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Home  > 2-((1R,5S,6S)-6-(aminomethyl)-3-ethylbicyclo[3.2.0]hept-3-en-6-yl)acetic acid

AE26537

1138245-13-2 | 2-((1R,5S,6S)-6-(aminomethyl)-3-ethylbicyclo[3.2.0]hept-3-en-6-yl)acetic acid

Packsize Purity Availability Price Discounted Price    Quantity
1mg 97% in stock $88.00 $62.00 -   +
100mg 97% in stock $163.00 $114.00 -   +
250mg 97% in stock $251.00 $176.00 -   +
1g 97% in stock $558.00 $391.00 -   +
5g 97% in stock $1,879.00 $1,316.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE26537
Chemical Name: 2-((1R,5S,6S)-6-(aminomethyl)-3-ethylbicyclo[3.2.0]hept-3-en-6-yl)acetic acid
CAS Number: 1138245-13-2
Molecular Formula: C12H19NO2
Molecular Weight: 209.28476000000003
MDL Number: MFCD28411425
SMILES: CCC1=C[C@@H]2[C@H](C1)C[C@]2(CN)CC(=O)O

 

Computed Properties
Complexity: 311  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 3  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 4  
XLogP3: -1.7  

 

 

Upstream Synthesis Route
  • The compound (1R,5S,6S)-6-(Aminomethyl)-3-ethylbicyclo[3.2.0]hept-3-ene-6-acetic acid, commonly referred to as $name$, serves as a versatile building block in chemical synthesis due to its unique structural features. In particular, this compound is valued for its ability to introduce a bicyclic framework with an amino-methyl moiety and an ethyl group into diverse organic molecules. When utilized in synthetic pathways, it can enable the creation of novel structures and functional groups that are key in the development of pharmaceuticals, agrochemicals, and materials science. By incorporating $name$ into synthetic routes, chemists can access a wide array of structurally complex and biologically active compounds, showcasing its significance in modern organic chemistry.
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