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CAS 1333319-47-3

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Methyl 2-(aminomethyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate

Description:
Methyl 2-(aminomethyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate, identified by its CAS number 1333319-47-3, is a chemical compound that features a benzoate structure with an aminomethyl group and a boron-containing moiety. This compound is characterized by its potential applications in organic synthesis, particularly in the field of medicinal chemistry and materials science. The presence of the dioxaborolane group suggests that it may participate in boron-mediated reactions, such as Suzuki coupling, which is valuable for forming carbon-carbon bonds. The tetramethyl substitution enhances its stability and solubility in organic solvents. Additionally, the aminomethyl group can serve as a functional handle for further chemical modifications, making it versatile for various synthetic pathways. Overall, this compound exemplifies the integration of boron chemistry with organic functional groups, highlighting its significance in developing new chemical entities and materials.
Formula:C15H22BNO4
InChI:InChI=1S/C15H22BNO4/c1-14(2)15(3,4)21-16(20-14)12-8-6-7-10(11(12)9-17)13(18)19-5/h6-8H,9,17H2,1-5H3
InChI key:InChIKey=HJJBSLWXNZXUIW-UHFFFAOYSA-N
SMILES:C(N)C1=C(C=CC=C1C(OC)=O)B2OC(C)(C)C(C)(C)O2
Synonyms:
  • Benzoic acid, 2-(aminomethyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, methyl ester
  • Methyl 2-(aminomethyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
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