CymitQuimica logo

CAS 186663-83-2

:

9H-Fluoren-9-ylmethyl N-(3-bromopropyl)carbamate

Description:
9H-Fluoren-9-ylmethyl N-(3-bromopropyl)carbamate, with the CAS number 186663-83-2, is an organic compound characterized by its unique structure that includes a fluorenyl group and a carbamate functional group. This compound typically exhibits properties associated with both the fluorenyl moiety, which is known for its stability and potential applications in organic electronics, and the bromopropyl group, which can enhance reactivity due to the presence of the bromine atom. The carbamate functional group contributes to the compound's solubility and potential for hydrogen bonding, making it useful in various chemical reactions and applications. It may also exhibit biological activity, making it of interest in medicinal chemistry. The compound is likely to be a solid at room temperature, with moderate solubility in organic solvents. Its synthesis and reactivity can be influenced by the presence of the bromine atom, which can participate in nucleophilic substitution reactions. Overall, this compound represents a versatile building block in organic synthesis and materials science.
Formula:C18H18BrNO2
InChI:InChI=1S/C18H18BrNO2/c19-10-5-11-20-18(21)22-12-17-15-8-3-1-6-13(15)14-7-2-4-9-16(14)17/h1-4,6-9,17H,5,10-12H2,(H,20,21)
InChI key:InChIKey=XWBHEIFHCNVXPS-UHFFFAOYSA-N
SMILES:C(OC(NCCCBr)=O)C1C=2C(C=3C1=CC=CC3)=CC=CC2
Synonyms:
  • 9H-Fluoren-9-ylmethyl N-(3-bromopropyl)carbamate
  • 9H-fluoren-9-ylmethyl (3-bromopropyl)carbamate
  • Carbamic acid, (3-bromopropyl)-, 9H-fluoren-9-ylmethyl ester
  • Carbamic acid, N-(3-bromopropyl)-, 9H-fluoren-9-ylmethyl ester
  • Fluorenylmethyl N-(3-Bromopropyl)Carbamate
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.