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CAS 590417-56-4

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1-Methyl-1H-indole-4-boronic acid

Description:
1-Methyl-1H-indole-4-boronic acid, with the CAS number 590417-56-4, is an organic compound that features a boronic acid functional group attached to an indole structure. This compound is characterized by its ability to form reversible covalent bonds with diols, making it useful in various applications, particularly in medicinal chemistry and organic synthesis. The presence of the boronic acid group allows for participation in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, the methyl group at the 1-position of the indole ring influences its electronic properties and solubility. The compound is typically a solid at room temperature and may exhibit moderate stability under standard conditions. Its reactivity and functional versatility make it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Safety data should be consulted for handling, as boronic acids can have specific toxicity profiles. Overall, 1-Methyl-1H-indole-4-boronic acid is an important building block in organic chemistry.
Formula:C9H10BNO2
InChI:InChI=1S/C9H10BNO2/c1-11-6-5-7-8(10(12)13)3-2-4-9(7)11/h2-6,12-13H,1H3
InChI key:InChIKey=GLLDFWAZHLTQLC-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C2C(N(C)C=C2)=CC=C1
Synonyms:
  • (1-Methyl-1H-indol-4-yl)boronic acid
  • B-(1-Methyl-1H-indol-4-yl)boronic acid
  • Boronic acid, (1-methyl-1H-indol-4-yl)-
  • Boronic acid, B-(1-methyl-1H-indol-4-yl)-
  • 1-Methyl-1H-indole-4-boronic acid
  • 1-Methy-1H-indol-4-ylboronic acid
  • 1-Methyl-1H-indol-4-yl hydrogen boronate
  • 1-Methylindole-4-boronic acid
  • (1-methyl-4-indolyl)boronic acid
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