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Home  > Chemistry  > Heterocyclic Building Blocks  > Thiophenes  > 5-Methoxycarbonyl-2-methylthiophene-3-boronic acid pinacol ester

AD65178

1109284-49-2 | 5-Methoxycarbonyl-2-methylthiophene-3-boronic acid pinacol ester

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $142.00 $99.00 -   +
500mg 95% in stock $280.00 $196.00 -   +
1g 95% in stock $401.00 $281.00 -   +
5g 95% in stock $1,879.00 $1,316.00 -   +
10g 95% in stock $2,811.00 $1,968.00 -   +

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*All prices are in USD.

Description
Catalog Number: AD65178
Chemical Name: 5-Methoxycarbonyl-2-methylthiophene-3-boronic acid pinacol ester
CAS Number: 1109284-49-2
Molecular Formula: C13H19BO4S
Molecular Weight: 282.16355999999996
MDL Number: MFCD18427556
SMILES: COC(=O)c1cc(c(s1)C)B1OC(C(O1)(C)C)(C)C

 

Computed Properties
Complexity: 356  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 19  
Hydrogen Bond Acceptor Count: 5  
Rotatable Bond Count: 3  

 

 

Upstream Synthesis Route
  • Methyl 5-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylate is a versatile compound widely used in chemical synthesis as a key building block. It serves as an essential reagent in the construction of various organic compounds, particularly in the formation of complex heterocyclic structures. This compound is commonly employed in the preparation of pharmaceutical intermediates, agrochemicals, and materials science applications. Its unique structure and reactivity make it a valuable tool for organic chemists seeking to efficiently create diverse molecular architectures with high precision and control. By incorporating Methyl 5-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylate into their synthetic routes, researchers can access novel chemical entities with potential relevance in drug discovery, material design, and other scientific endeavors.
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