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CAS 107474-79-3

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(+)-1-(9-FLUORENYL)ETHYL CHLOROFORMATE

Description:
(+)-1-(9-Fluorenyl)ethyl chloroformate is an organic compound characterized by its chloroformate functional group, which is known for its reactivity in various chemical transformations. This compound features a fluorenyl moiety, contributing to its unique structural and electronic properties. The presence of the chloroformate group makes it a useful reagent in organic synthesis, particularly in the formation of esters and in the protection of alcohols. The stereochemistry indicated by the "(+)" prefix suggests that this compound is optically active, which may influence its reactivity and interactions in chiral environments. Additionally, the compound's molecular structure allows for potential applications in medicinal chemistry and materials science, where the fluorenyl group can impart specific characteristics such as fluorescence or enhanced stability. As with many chloroformates, it is important to handle this substance with care due to its potential reactivity and toxicity, particularly in the presence of nucleophiles. Overall, (+)-1-(9-fluorenyl)ethyl chloroformate is a valuable compound in synthetic organic chemistry.
Formula:C16H13ClO2
InChI:InChI=1/C16H13ClO2/c1-10(19-16(17)18)15-13-8-4-2-6-11(13)12-7-3-5-9-14(12)15/h2-10,15H,1H3/t10-/m1/s1
SMILES:C[C@H](C1c2ccccc2c2ccccc12)OC(=O)Cl
Synonyms:
  • (-)-Flec Solution,50 Mg In 10 Ml Acetone
  • (+)-Flec(Tm)
  • (-)-Flec(R)
  • (-)-Flec
  • (-)-1-(9-Fluorenyl)ethylchloroformate
  • 1-(9H-fluoren-9-yl)ethyl carbonochloridate
  • (1S)-1-(9H-fluoren-9-yl)ethyl chlorocarbonate
  • (1R)-1-(9H-fluoren-9-yl)ethyl chlorocarbonate
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