15724-87-5

Usage

InChI:InChI=1/C10H9ClO2/c1-13-9-4-2-8(3-5-9)10(12)6-7-11/h2-7H,1H3/b7-6+

Upstream product

• 16469-68-4 1-(4-methoxyphenyl)-2-propyn-1-one 
• 75-01-4 chloroethylene 
• 100-07-2 4-methoxy-benzoyl chloride 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 109-94-4 formic acid ethyl ester 
• 68996-68-9 3,3-dichloro-1-(4-methoxy-phenyl)-propan-1-one 

Downstream Products

• 37670-76-1 {[(E)-3-(4-Methoxy-phenyl)-3-oxo-propenyl]-methyl-amino}-acetic acid ethyl ester 
• 54556-81-9 (cis-2-Thiocyanatovinyl)-(4-methoxyphenyl)-keton 
• 22079-79-4 trans-N-Methyl-N,N-bis-<2-chlor-aethyl>-N-<2-(4-methoxy-benzoyl)-vinyl>-ammoniumchlorid 
• 68996-69-0 (E)-1-Chloro-3-(4-methoxy-phenyl)-pent-1-en-4-yn-3-ol 
• 83241-54-7 Morpholine-4-carboximidothioic acid (Z)-3-(4-methoxy-phenyl)-3-oxo-propenyl ester; compound with perchloric acid 
• 83241-74-1 N-Phenyl-morpholine-4-carboximidothioic acid (Z)-3-(4-methoxy-phenyl)-3-oxo-propenyl ester; compound with perchloric acid 
• 83241-30-9 2-[(Z)-3-(4-Methoxy-phenyl)-3-oxo-propenyl]-1,1-dimethyl-isothiourea; compound with perchloric acid 
• 83241-20-7 2-[(Z)-3-(4-Methoxy-phenyl)-3-oxo-propenyl]-isothiourea; compound with perchloric acid 
• 83241-84-3 N-[(E)-3-(4-Methoxy-phenyl)-3-oxo-propenyl]-N-phenyl-thiobenzamide 
• 68996-70-3 3-(p-Methoxyphenyl)-2-penten-4-ynal 
• 68996-76-9 (2E,4Z)-1,5-Bis-(4-methoxy-phenyl)-hepta-2,4-dien-6-yn-1-one 
• 83251-66-5 N-Phenyl-thiobenzimidic acid (Z)-3-(4-methoxy-phenyl)-3-oxo-propenyl ester; compound with perchloric acid 
• 83241-78-5 N-Phenyl-thiobenzimidic acid (Z)-3-(4-methoxy-phenyl)-3-oxo-propenyl ester 

Relevant academic research and scientific papers

A new route for the synthesis of bisunsaturated oxosulfones and bissulfones under Friedel Craft's conditions

A new class of 1-aroyl-2-styrylsulfonylethenes 4 and 1-arylsulfonyl-2-styrylsulfonylethenes 5 has been reported.

A novel method for the synthesis of aromatic E-β-chlorovinylketones

The reaction of aromatic acetylenic ketones with aqueous HCl promoted by catalytic FeSO4 gave a E,Zmixture of β-chlorovinylketones which isomerized almost exclusively to the E-β-isomer upon heating. (C) 2000 Elsevier Science Ltd.

Ferroelectric liquid crystal compounds containing chiral haloalkoxy tail units and compositions containing them

Chiral, nonracemic compounds of the general formula: STR1 wherein m and n are either both zero, both equal one or n is equal to one and m is equal to zero, X and Y and Z are halogens, R' is an alkyl, alkoxyl, alkenyl, thioalkyl, thioether, ether, or alkylsilyl group containing three to fifteen carbon atoms, and R is an alkyl group having one to fifteen carbon atoms and where Ar is: where A, B and D independently of one another are aromatic rings which are selected from the group consisting of a phenyl, a pyridine ring, a pyrimidine ring, a pyridizine ring, a pyrazine ring and a thiadiazole ring, wherein a, b and d are integers from 0-3 such that a+b+d=2-3, where E and F independently of one another are linking groups selected from the group consisting of a --CH2 --CH2 --, --CH2 --O--, --CH2 --S--, --O--CH2 --, --S--CH2, --OOC-- or --COO-- wherein e and f can be 1 or 0, when e and/or f is 0, the adjacent aromatic rings are linked by a carbon-carbon single bond, preferably e and f are both 0 or one of e or f is 1, and wherein * indicates a chiral center, which are useful as ferroelectric liquid crystal components having high polarization are described.