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Preparation and characterization of diazenyl quinolin-8-ol with trifluoromethyl substituents

Mohammad R Yazdanbakhsh 1
Mohammad R Yazdanbakhsh
, 
Nosrat Ollah Mahmoodi 1
Nosrat Ollah Mahmoodi
, 
Shahram Dabiry 1
Shahram Dabiry
10.1070/MC2006v016n03ABEH002331
Published 2006-07-06
Communication , Volume 16, Issue 3, 192-194
11
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Yazdanbakhsh M. R., Mahmoodi N. O., Dabiry S. Preparation and characterization of diazenyl quinolin-8-ol with trifluoromethyl substituents // Mendeleev Communications. 2006. Vol. 16. No. 3. pp. 192-194.
GOST all authors (up to 50) Copy
Yazdanbakhsh M. R., Mahmoodi N. O., Dabiry S. Preparation and characterization of diazenyl quinolin-8-ol with trifluoromethyl substituents // Mendeleev Communications. 2006. Vol. 16. No. 3. pp. 192-194.
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TY - JOUR
DO - 10.1070/MC2006v016n03ABEH002331
UR - https://mendcomm.colab.ws/publications/10.1070/MC2006v016n03ABEH002331
TI - Preparation and characterization of diazenyl quinolin-8-ol with trifluoromethyl substituents
T2 - Mendeleev Communications
AU - Yazdanbakhsh, Mohammad R
AU - Mahmoodi, Nosrat Ollah
AU - Dabiry, Shahram
PY - 2006
DA - 2006/07/06
PB - Mendeleev Communications
SP - 192-194
IS - 3
VL - 16
ER -
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@article{2006_Yazdanbakhsh,
author = {Mohammad R Yazdanbakhsh and Nosrat Ollah Mahmoodi and Shahram Dabiry},
title = {Preparation and characterization of diazenyl quinolin-8-ol with trifluoromethyl substituents},
journal = {Mendeleev Communications},
year = {2006},
volume = {16},
publisher = {Mendeleev Communications},
month = {Jul},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2006v016n03ABEH002331},
number = {3},
pages = {192--194},
doi = {10.1070/MC2006v016n03ABEH002331}
}
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Yazdanbakhsh, Mohammad R., et al. “Preparation and characterization of diazenyl quinolin-8-ol with trifluoromethyl substituents.” Mendeleev Communications, vol. 16, no. 3, Jul. 2006, pp. 192-194. https://mendcomm.colab.ws/publications/10.1070/MC2006v016n03ABEH002331.

Abstract

The synthesis and properties of new monoazo dyes derived from the diazonium salts of 2-trifluoromethyl phenylamine and 4-chloro-3-trifluoromethyl phenylamine are considered.

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