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CAS 669713-57-9

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2-[[(1,1-Dimethylethoxy)carbonyl]amino]-3,5-dimethylbenzoic acid

Description:
2-[[(1,1-Dimethylethoxy)carbonyl]amino]-3,5-dimethylbenzoic acid, with the CAS number 669713-57-9, is a chemical compound characterized by its complex structure, which includes a benzoic acid moiety substituted with both dimethyl groups and an amino group that is further modified by a dimethylethoxycarbonyl group. This compound typically exhibits properties associated with both aromatic and carboxylic acid functionalities, such as potential acidity due to the carboxylic acid group and hydrophobic characteristics from the aromatic ring and alkyl substituents. Its molecular structure suggests it may participate in various chemical reactions, including amide formation and esterification, and it may also exhibit biological activity, making it of interest in pharmaceutical research. The presence of the dimethylethoxycarbonyl group can enhance solubility and stability, which are important for its application in drug development. Overall, this compound's unique structural features contribute to its potential utility in various chemical and biological contexts.
Formula:C14H19NO4
InChI:InChI=1S/C14H19NO4/c1-8-6-9(2)11(10(7-8)12(16)17)15-13(18)19-14(3,4)5/h6-7H,1-5H3,(H,15,18)(H,16,17)
InChI key:InChIKey=ITWQZQYNZFDETR-UHFFFAOYSA-N
SMILES:N(C(OC(C)(C)C)=O)C1=C(C(O)=O)C=C(C)C=C1C
Synonyms:
  • 2-Tert-Butoxycarbonylamino-3,5-Dimethylbenzoicacid
  • 2-[[(1,1-Dimethylethoxy)carbonyl]amino]-3,5-dimethylbenzoic acid
  • Benzoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-3,5-dimethyl-
  • 2-((tert-Butoxycarbonyl)amino)-3,5-dimethylbenzoic acid
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