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Home  > methyl 1-[3-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]cyclopropane-1-carboxylate

AI04908

1004294-83-0 | methyl 1-[3-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]cyclopropane-1-carboxylate

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $289.00 $202.00 -   +
1g 95% in stock $867.00 $607.00 -   +
5g 95% in stock $3,432.00 $2,403.00 -   +

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*All prices are in USD.

Description
Catalog Number: AI04908
Chemical Name: methyl 1-[3-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]cyclopropane-1-carboxylate
CAS Number: 1004294-83-0
Molecular Formula: C17H23BO4
Molecular Weight: 302.17312
MDL Number: MFCD18761349
SMILES: COC(=O)C1(CC1)c1cccc(c1)B1OC(C(O1)(C)C)(C)C

 

Computed Properties
Complexity: 440  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 22  
Hydrogen Bond Acceptor Count: 4  
Rotatable Bond Count: 4  

 

 

Upstream Synthesis Route
  • The chemical compound, methyl 1-[3-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]cyclopropane-1-carboxylate, serves as a valuable reagent in chemical synthesis due to its unique structural properties. This compound is commonly employed as a versatile precursor in the synthesis of various organic molecules, particularly in the field of medicinal and pharmaceutical chemistry.One key application of this compound lies in its ability to serve as a building block for the construction of complex organic frameworks. By utilizing the functional groups present in its structure, chemists can modify and transform this compound into a diverse array of derivatives through selective chemical reactions. These derivatives can then be further elaborated to create novel drug candidates, agrochemicals, or materials with tailored properties.Furthermore, the presence of the tetramethyl-1,3,2-dioxaborolane moiety in the molecule enables chemists to harness the unique reactivity of boron in organic synthesis. Boron-containing compounds are widely used as versatile reagents in various cross-coupling reactions, allowing for efficient and selective bond formation between different molecular fragments. Through judicious manipulation of the boron center, chemists can access structural motifs that are challenging to achieve with traditional organic chemistry methods.Overall, the application of methyl 1-[3-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]cyclopropane-1-carboxylate in chemical synthesis offers a powerful toolbox for synthetic chemists to access novel molecular architectures and facilitate the development of innovative molecules with potential applications in drug discovery and materials science.
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