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Home  > Pyrano[3,4-b]indole-1-acetic acid, 1,8-diethyl-1,3,4,9-tetrahydro-, methyl ester

AA55410

122188-02-7 | Pyrano[3,4-b]indole-1-acetic acid, 1,8-diethyl-1,3,4,9-tetrahydro-, methyl ester

Packsize Purity Availability Price Discounted Price    Quantity
5mg 98% in stock $80.00 $56.00 -   +
25mg 98% in stock $151.00 $106.00 -   +
100mg 98% in stock $309.00 $217.00 -   +
500mg 98% in stock $779.00 $546.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA55410
Chemical Name: Pyrano[3,4-b]indole-1-acetic acid, 1,8-diethyl-1,3,4,9-tetrahydro-, methyl ester
CAS Number: 122188-02-7
Molecular Formula: C18H23NO3
Molecular Weight: 301.3801
MDL Number: MFCD02684434
SMILES: COC(=O)CC1(CC)OCCc2c1[nH]c1c2cccc1CC

 

Computed Properties
Complexity: 413  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 22  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 5  
Undefined Atom Stereocenter Count: 1  
XLogP3: 3.1  

 

 

Upstream Synthesis Route
  • Methyl 2-(1,8-diethyl-1,3,4,9-tetrahydropyrano[3,4-b]indol-1-yl)acetate is a versatile compound used in chemical synthesis for its unique reactivity and structural properties. In organic synthesis, it serves as a valuable building block for the creation of complex molecules due to its functional groups and structural features. This compound can participate in various reactions such as acylation, alkylation, and cyclization to form diverse chemical products. Its presence in a reaction pathway can lead to the formation of novel compounds with potential applications in pharmaceuticals, materials science, and other industries. Additionally, the specific arrangement of atoms in this compound allows for selective modification at different positions, enabling precise control over the desired chemical transformations. As a result, Methyl 2-(1,8-diethyl-1,3,4,9-tetrahydropyrano[3,4-b]indol-1-yl)acetate plays a crucial role in advancing the field of chemical synthesis by facilitating the creation of new molecules with targeted properties and functions.
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