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Home  > 4-Hexenoic acid, 6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-, sodium salt(1:1) , (4E)-

AB52739

37415-62-6 | 4-Hexenoic acid, 6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-, sodium salt(1:1) , (4E)-

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $156.00 $109.00 -   +
1g 95% in stock $530.00 $371.00 -   +

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Description
Catalog Number: AB52739
Chemical Name: 4-Hexenoic acid, 6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-, sodium salt(1:1) , (4E)-
CAS Number: 37415-62-6
Molecular Formula: C17H19NaO6
Molecular Weight: 342.3189
MDL Number: MFCD01723176
SMILES: COc1c(C/C=C(/CCC(=O)[O-])C)c(O)c2c(c1C)COC2=O.[Na+]

 

Computed Properties
Complexity: 492  
Covalently-Bonded Unit Count: 2  
Defined Bond Stereocenter Count: 1  
Heavy Atom Count: 24  
Hydrogen Bond Acceptor Count: 6  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 6  

 

 

Upstream Synthesis Route 
  • 4-Hexenoic acid, 6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-, sodium salt(1:1), (4E)- serves as a valuable reagent in chemical synthesis due to its unique structural characteristics. This compound is commonly utilized as a key building block for the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its specific functional groups make it a versatile intermediate in organic reactions, enabling the formation of complex molecular structures through processes such as esterification, hydrolysis, and alkylation. Additionally, the sodium salt form of this compound promotes enhanced solubility and reactivity in aqueous solutions, facilitating its incorporation in a wide range of synthetic pathways.
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