Products
4-(Chlorodifluoromethoxy)aniline
Another name：4-(CHLORO-DIFLUORO-METHOXY)-PHENYLAMINE;
CasNo: 39065-95-7 Purity： ≥99% Molecular Structure： C7H6ClF2NO
4-(Chlorodifluoromethoxy)aniline Basic Product Information
| Product Name |
4-(Chlorodifluoromethoxy)aniline |
CAS | 39065-95-7 |
| Synonyms | 4-(CHLORO-DIFLUORO-METHOXY)-PHENYLAMINE; | Molecular Formula | C7H6ClF2NO |
| EINECS Number | / | Molecular Structure | |
| Appearance | Yellow liquid |
 |
|
| Purity | ≥99% | ||
| Supply Ability | 1T / Per Month | ||
4-(Chlorodifluoromethoxy)aniline Appearance/Package/Shipping/Storage
Package
25kg/Drum
Storage condition
Preserve in well-closed containers, and store at room temperature.
4-(Chlorodifluoromethoxy)aniline Application
Intermediate for pharmaceutical or pesticide synthesis;
4-(Chlorodifluoromethoxy)aniline literature
Synergistic effects in Fe nanoparticles doped with ppm levels of (Pd + Ni). A new catalyst for sustainable nitro group reductions
Pang, Haobo,Gallou, Fabrice,Sohn, Hyuntae,Camacho-Bunquin, Jeffrey,Delferro, Massimiliano,Lipshutz, Bruce H.
supporting information, p. 130 - 135 (2018/01/12)
A remarkable synergistic effect has been uncovered between ppm levels of Pd and Ni embedded within iron nanoparticles that leads to mild and selective catalytic reductions of nitro-containing aromatics and heteroaromatics in water at room temperature. NaBH4 serves as the source of inexpensive hydride. Broad substrate scope is documented, along with several other features including: low catalyst loading, low residual metal in the products, and recycling of the catalyst and reaction medium, highlight the green nature of this new technology.
A 4 - ( chlorine two fluorine methoxy ) method for preparing aniline
-
, (2018/02/04)
The invention relates to a preparation method for 4-(chlorodifluoromethoxy)aniline. The method includes: taking trichloromethoxybenzene as the raw material, employing hydrogen fluoride to conduct selective fluorination to obtain chlorodifluoromethoxybenze
Hydrogenation on granular palladium-containing catalysts: II. Hydrogenation of nitroheterocyclic compounds
Kislyi,Tolkacheva,Semenov
, p. 269 - 271 (2007/10/03)
Nitroheterocyclic compounds were reduced in a classical reactor with an agitator equipped with a cell for fixed bed of catalyst. As catalysts were applied granular palladium catalysts (0.5% of Pd on γ-Al2O 3 and 2% of Pd on granulated carbon). Anilines and 3-amino-2(1H)-pyridones were obtained in high yield at reduction of the appropriate nitro compounds, and the activity of the catalyst samples only slightly decreased. Yet aminopyrazoles and aminoimidazoles obtained by hydrogenation on palladium were very sensitive to the presence of air even as hydrochlorides. In the course of hydrogenation of nitropyrazoles and nitroimidazoles the activity of the catalyst markedly decreased.
4-(Chlorodifluoromethoxy)aniline Upstream and downstream
39065-95-7 Upstream product
40750-71-8
1-(chlorodifluoromethoxy)-4-nitrobenzene
34888-05-6
(trichloromethoxy)benzene
39065-95-7 Downstream Products
40750-71-8
1-(chlorodifluoromethoxy)-4-nitrobenzene
34888-05-6
(trichloromethoxy)benzene
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