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CAS 88235-25-0

:

6-[N-(7-Nitrobenz-2-oxa-1,3-diazol-4-yl)amino]hexanoic acid

Description:
6-[N-(7-Nitrobenz-2-oxa-1,3-diazol-4-yl)amino]hexanoic acid, commonly referred to as a fluorescent probe, is characterized by its unique structure that combines a hexanoic acid chain with a nitrobenzoxadiazole moiety. This compound is known for its fluorescent properties, making it useful in various biochemical applications, particularly in labeling and imaging studies. The presence of the nitrobenzoxadiazole group contributes to its strong fluorescence, which is often utilized in biological assays to track molecular interactions or cellular processes. The hexanoic acid portion provides a hydrophobic character, enhancing its ability to penetrate biological membranes. Additionally, this compound may exhibit solubility in organic solvents and limited solubility in water, depending on the pH and the presence of other solubilizing agents. Its stability and reactivity can be influenced by environmental conditions, such as light and temperature, which are important considerations for its application in experimental settings. Overall, this compound serves as a valuable tool in the field of molecular biology and biochemistry.
Formula:C12H14N4O5
InChI:InChI=1S/C12H14N4O5/c17-10(18)4-2-1-3-7-13-8-5-6-9(16(19)20)12-11(8)14-21-15-12/h5-6,13H,1-4,7H2,(H,17,18)
InChI key:InChIKey=DJFNQJJTTPMBIL-UHFFFAOYSA-N
SMILES:N(CCCCCC(O)=O)C=1C=2C(C(N(=O)=O)=CC1)=NON2
Synonyms:
  • 2,1,3-Benzoxadiazole, hexanoic acid deriv.
  • 6-(N-(7-Nitrobenz-2-oxa-1,3-diazol- 4-yl)amino)hexanoic acid (NBD-X)
  • 6-[(7-Nitro-2,1,3-Benzoxadiazol-4-Yl)Amino]Hexanoic Acid
  • 6-[(7-Nitrobenzofurazan-4-yl)amino]hexanoic acid
  • 6-[N-(7-Nitrobenz-2-oxa-1,3-diazol-4-yl)amino]hexanoic acid
  • 6-t-7-Nitrobenzofurazan-4-ylaminohexanoic acid
  • C6-Nbd
  • Hexanoic acid, 6-[(7-nitro-2,1,3-benzoxadiazol-4-yl)amino]-
  • Hexanoic acid, 6-[(7-nitro-4-benzofurazanyl)amino]-
  • N 316
  • See more synonyms
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