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3-(4-Bromophenyl)-2-ethylacrylic acid

✍ Scribed by Muhammad, Niaz ;Zia-ur-Rehman, ;Ali, Saqib ;Meetsma, Auke


Book ID
104490734
Publisher
International Union of Crystallography
Year
2007
Tongue
English
Weight
150 KB
Volume
63
Category
Article
ISSN
1600-5368

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3-(4-Bromophenyl)-2-methylacrylic acid
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(E)-2-(4-Bromophenyl)-3-o-tolylacrylic a
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The solid-state structure of the title compound, C 16 H 13 BrO 2 , demonstrates an E configuration about the central C C bond. Symmetry-related molecules are linked by O-HÁ Á ÁO hydrogen bonds [OÁ Á ÁO = 2.617 (3) A ˚], forming centrosymmetric carboxylic acid dimers.

2-[5-(4-Bromophenyl)-3-methylsulfanyl-1-
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The title compound, C~17~H~13~BrO~3~S, was prepared by alkaline hydrolysis of ethyl 2-[5-(4-bromophenyl)-3-methylsulfanyl-1-benzofuran-2-yl]acetate. There are two symmetry-independent molecules in the asymmetric unit. The 4-bromophenyl rings are rotated out of the benzofuran planes, with dihedral an

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The title compound, C 25 H 16 BrN, was synthesized by the reaction of N-arylidenenaphthalen-2-amine and phenylacetaldehyde in the presence of iodine. In the molecular structure, the benzoquinoline ring system makes dihedral angles of 61.1 (1) and 39.8 (1) , respectively, with the phenyl and bromophe