Ad
related to: chlorobenzene to 2 chloroacetophenone c 1 10
Search results
Results From The WOW.Com Content Network
Phenacyl chloride, also commonly known as chloroacetophenone, is a substituted acetophenone. It is a useful building block in organic chemistry . Apart from that, it has been historically used as a riot control agent , where it is designated CN . [ 5 ]
This page was last edited on 31 January 2024, at 19:46 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
88.5–89 °C (191.3–192.2 °F; 361.6–362.1 K) Except where otherwise noted, ... Chloroacetophenone oxime is the oxime derivative of chloroacetophenone.
Chlorobenzene once was used in the manufacture of pesticides, most notably DDT, by reaction with chloral (trichloroacetaldehyde), but this application has declined with the diminished use of DDT. At one time, chlorobenzene was the main precursor for the manufacture of phenol: [10] C 6 H 5 Cl + NaOH → C 6 H 5 OH + NaCl
1,10-Phenanthroline is an inhibitor of metallopeptidases, with one of the first observed instances reported in carboxypeptidase A. [11] Inhibition of the enzyme occurs by removal and chelation of the metal ion required for catalytic activity, leaving an inactive apoenzyme . 1,10-Phenanthroline targets mainly zinc metallopeptidases, with a much ...
Acetophenone is formed as a byproduct of the cumene process, the industrial route for the synthesis of phenol and acetone.In the Hock rearrangement of isopropylbenzene hydroperoxide, migration of a methyl group rather than the phenyl group gives acetophenone and methanol as a result of an alternate rearrangement of the intermediate:
It is treated with aqueous sodium hydroxide at 350 °C and 300 bar or molten sodium hydroxide at 350 °C to convert it to sodium phenoxide, which yields phenol upon acidification. [2] When 1-[14 C]-1-chlorobenzene was subjected to aqueous NaOH at 395 °C, ipso substitution product 1-[14 C]-phenol was formed in 54% yield, while cine substitution ...
The use of chiral alcohol (R)-(+)-sec-o-bromophen-ethyl alcohol gave 82%ee (percent enantiomeric excess) in the reduction of 2-chloroacetophenone. [8] This enantioselection is due to the sterics of the two phenol groups in the six membered transition state as shown in Figure 3.