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CAS 133950-70-6

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5-BROMO-3-INDOXYL NONANOATE

Description:
5-Bromo-3-indoxyl nonanoate is a chemical compound characterized by its structure, which includes a bromine atom and an indoxyl moiety linked to a nonanoate chain. This compound is typically used in biochemical applications, particularly as a substrate in enzyme assays, due to its ability to produce a colored product upon enzymatic cleavage. The presence of the bromine atom enhances its reactivity and specificity in various chemical reactions. The nonanoate portion contributes to its lipophilicity, allowing it to interact effectively with biological membranes. In terms of solubility, it is generally soluble in organic solvents but may have limited solubility in water, which is a common trait for many indoxyl derivatives. Safety data for this compound should be consulted, as it may pose hazards typical of brominated organic compounds. Overall, 5-bromo-3-indoxyl nonanoate serves as a valuable tool in molecular biology and biochemistry for studying enzyme activity and other biochemical processes.
Formula:C17H22BrNO2
InChI:InChI=1/C17H22BrNO2/c1-2-3-4-5-6-7-8-17(20)21-16-12-19-15-10-9-13(18)11-14(15)16/h9-12,19H,2-8H2,1H3
SMILES:CCCCCCCCC(=O)Oc1c[nH]c2ccc(cc12)Br
Synonyms:
  • Rarechem Ah Bs 0021
  • Blue-Nonanoate
  • Lapis(Tm)-Nonanoate
  • 5-Bromo-3-Indolyl Nonanoate
  • 5-bromo-1H-indol-3-yl nonanoate
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