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CAS 1611-03-6

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3,5-Bis(1,1-dimethylethyl)-4-hydroxybenzeneacetic acid

Description:
3,5-Bis(1,1-dimethylethyl)-4-hydroxybenzeneacetic acid, also known as a derivative of a phenolic compound, is characterized by its unique structure that includes a hydroxy group and a carboxylic acid functional group, contributing to its potential as an antioxidant. The presence of two bulky tert-butyl groups at the 3 and 5 positions of the aromatic ring enhances its lipophilicity, which can influence its solubility and reactivity in various environments. This compound is often studied for its biological activities, including potential anti-inflammatory and antioxidant properties, making it of interest in pharmaceutical and cosmetic applications. Its CAS number, 1611-03-6, allows for easy identification in chemical databases. Additionally, the compound's stability and reactivity can be affected by factors such as pH and temperature, which are important considerations in its practical applications. Overall, 3,5-Bis(1,1-dimethylethyl)-4-hydroxybenzeneacetic acid represents a significant class of compounds with diverse applications in chemistry and biochemistry.
Formula:C16H24O3
InChI:InChI=1S/C16H24O3/c1-15(2,3)11-7-10(9-13(17)18)8-12(14(11)19)16(4,5)6/h7-8,19H,9H2,1-6H3,(H,17,18)
InChI key:InChIKey=QLMGIWHWWWXXME-UHFFFAOYSA-N
SMILES:C(C)(C)(C)C1=C(O)C(C(C)(C)C)=CC(CC(O)=O)=C1
Synonyms:
  • (3,5-Di-Tert-Butyl-4-Hydroxyphenyl)Acetate
  • (4-Hydroxy-3,5-di-tert-butylphenyl)acetic acid
  • 2,6-Di-tert-butyl-4-(carboxymethyl)phenol
  • 3,5-Bis(1,1-dimethylethyl)-4-hydroxybenzeneacetic acid
  • 3,5-Di-tert-butyl-4-hydroxyphenylacetic acid
  • Acetic acid, (3,5-di-tert-butyl-4-hydroxyphenyl)-
  • Benzeneacetic acid, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-
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