(S)-1-(2-Chlorophenyl)-2-oxocyclohexan-1-aminiumD-tartrate

(S)-1-(2-Chloro­phen­yl)-2-oxocyclo­hexan-1-aminium d-tartrate

In the title compound, C(12)H(15)ClNO(+)·C(4)H(5)O(6) (-), the cyclo-hexa-none ring adopts a chair conformation. The benzene ring is significantly twisted so that it is in an almost perpendicular position to the C-N bond with a C(Ar)-C(Ar)-C-N torsion angle of -96.5 (5)°. Intermolecular N-H⋯O and O-H⋯O hydrogen bonds are observed in the crystal structure.

1:1:1-Trichloro-2:2-di-(p-chlorophenyl)ethane (DDT) and rat adipose tissue.

E ) - 1 - ( 2 - Aminophenyl ) - 3 - ( 4 - chlorophenyl ) prop - 2 - en - 1 - one

The title chalcone (E)-1-(2-aminophenyl)-3-(4-chlorophenyl)prop-2-en-1-one was prepared with an excellent yield from a Claisen–Schmidt condensation reaction between o-aminoacetophenone and p-chlorobenzaldehyde. This product will be used as a key precursor for the development of an alternative route for the total synthesis of dubamine and graveoline alkaloids. Single crystals of the title compou...

(4-Chlorophenyl)(2-hydroxy-7-methoxynaphthalen-1-yl)methanone

The title compound, C(18)H(13)ClO(3), has an intra-molecular O-H⋯O=C hydrogen bond between the carbonyl group and the hydr-oxy substituent on the naphthalene ring system. The angle between the C=O bond plane and the naphthalene ring system is relatively small [20.96 (8)°]. The angle between the benzene ring and the carbonyl group is rather large [35.65 (9)°] compared to that in an analogous com...

Photosynthesis-Inhibiting Activity of 1-[(2-Chlorophenyl)carbamoyl]- and 1-[(2-Nitrophenyl)carbamoyl]naphthalen-2-yl Alkylcarbamates.

Eight 1-[(2-chlorophenyl)carbamoyl]naphthalen-2-yl alkylcarbamates and eight 1-[(2-nitrophenyl)carbamoyl]naphthalen-2-yl alkylcarbamates were tested for their activity related to the inhibition of photosynthetic electron transport (PET) in spinach (Spinacia oleracea L.) chloroplasts. The PET-inhibiting activity of the compounds was relatively low; the corresponding IC50 values ranged from 0.05 ...