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Home  > Chemistry  > Organic Building Blocks  > Phenols  > 2,6-dichloro-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

AA01893

1003298-87-0 | 2,6-dichloro-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

Packsize Purity Availability Price Discounted Price    Quantity
1g 97% in stock $33.00 $23.00 -   +
25g 97% in stock $620.00 $434.00 -   +

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Description
Catalog Number: AA01893
Chemical Name: 2,6-dichloro-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
CAS Number: 1003298-87-0
Molecular Formula: C12H15BCl2O3
Molecular Weight: 288.9627
MDL Number: MFCD20526385
SMILES: CC1(C)OB(OC1(C)C)c1cc(Cl)c(c(c1)Cl)O

 

Computed Properties
Complexity: 296  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 18  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 1  

 

 

Upstream Synthesis Route
  • The 2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In organic chemistry, this compound serves as a key building block for the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. It acts as a valuable reagent in the Suzuki-Miyaura cross-coupling reaction, allowing for the introduction of the phenolic group into complex molecular structures. Additionally, its boron moiety enables efficient C-C bond formation, making it a valuable tool in the construction of diverse organic molecules. Furthermore, the presence of the chloro and phenolic functionalities provides opportunities for further derivatization, enhancing its utility in designing novel compounds with specific properties. Overall, the application of 2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol in chemical synthesis underscores its significance in modern organic chemistry research and development.
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