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Home  > 2(1H)-Isoquinolinecarboxylic acid, 3,4-dihydro-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, 1,1-dimethylethyl ester

AH97078

937048-76-5 | 2(1H)-Isoquinolinecarboxylic acid, 3,4-dihydro-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, 1,1-dimethylethyl ester

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $49.00 $35.00 -   +
250mg 98% in stock $90.00 $63.00 -   +
1g 98% in stock $180.00 $126.00 -   +
5g 98% in stock $550.00 $385.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AH97078
Chemical Name: 2(1H)-Isoquinolinecarboxylic acid, 3,4-dihydro-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, 1,1-dimethylethyl ester
CAS Number: 937048-76-5
Molecular Formula: C20H30BNO4
Molecular Weight: 359.2675
MDL Number: MFCD11044674
SMILES: O=C(N1CCc2c(C1)cc(cc2)B1OC(C(O1)(C)C)(C)C)OC(C)(C)C

 

Upstream Synthesis Route
  • The tert-Butyl 7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate is a versatile compound utilized in chemical synthesis as a key building block for the introduction of the 1,3,2-dioxaborolane moiety into organic molecules. This functional group is highly valuable in modern organic synthesis due to its compatibility with a wide range of reaction conditions and its ability to undergo efficient transformations.Specifically, the tert-Butyl 7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate serves as a crucial intermediate for the selective installation of boron-containing groups in target molecules. The presence of the dioxaborolane moiety enables chemists to perform diverse chemical manipulations such as Suzuki-Miyaura cross-coupling reactions, which are fundamental in the construction of biaryl compounds. Additionally, the unique structural features of this compound make it a valuable tool for the development of new pharmaceuticals, agrochemicals, and materials with tailored properties.By incorporating tert-Butyl 7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate into synthetic routes, chemists can access a broad array of structurally complex molecules with enhanced functionalities and potential applications in various fields of chemistry and beyond.
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