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2-(4-Bromophenyl)-5-methyl-3-methylsulfinyl-1-benzofuran

✍ Scribed by Choi, Hong Dae ;Seo, Pil Ja ;Son, Byeng Wha ;Lee, Uk


Publisher
International Union of Crystallography
Year
2007
Tongue
English
Weight
1023 KB
Volume
63
Category
Article
ISSN
1600-5368

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📜 SIMILAR VOLUMES


2-(4-Bromophenyl)-5,7-dimethyl-3-methyls
✍ Choi, Hong Dae ;Seo, Pil Ja ;Son, Byeng Wha ;Lee, Uk 📂 Article 📅 2007 🏛 International Union of Crystallography 🌐 English ⚖ 578 KB

The title compound, C~17~H~15~BrO~2~S, was prepared by the oxidation of 2-(4-bromophenyl)-5,7-dimethyl-3-methylsulfanyl-1-benzofuran using 3-chloroperbenzoic acid. The 4-bromophenyl ring is rotated out of the benzofuran plane, with a dihedral angle of 19.3 (2)°. The O atom and the methyl group of th

5-(4-Bromo­phen­yl)-2-methyl-3-methyl­su
✍ Choi, Hong Dae ;Woo, Hyun Mi ;Seo, Pil Ja ;Son, Byeng Wha ;Lee, Uk 📂 Article 📅 2006 🏛 International Union of Crystallography 🌐 English ⚖ 171 KB

The title compound, C 16 H 13 BrOS, was prepared by the Lewis acid-catalysed reaction of 4 0 -bromo-1,1 0 -biphenyl-4-ol withchloro--(methylsulfanyl)acetone. The crystal structure is stabilized by a C-HÁ Á Á interaction involving a CH group of the 4-bromophenyl ring and the furan ring.

2-Methyl-3-methyl­sulfinyl-5-phenyl-1-be
✍ Choi, Hong Dae ;Seo, Pil Ja ;Lee, Hee Kyung ;Son, Byeng Wha ;Lee, Uk 📂 Article 📅 2006 🏛 International Union of Crystallography 🌐 English ⚖ 97 KB

The title compound, C 16 H 14 O 2 S, was prepared by oxidation of 2-methyl-3-methylsulfanyl-5-phenyl-1-benzofuran using 3chloroperbenzoic acid. Shortstacking distances are prevented by the steric influence of the methylsulfinyl group.

5-Chloro-2-methyl-3-methyl­sulfinyl-1-be
✍ Choi, Hong Dae ;Seo, Pil Ja ;Son, Byeng Wha ;Lee, Uk 📂 Article 📅 2007 🏛 International Union of Crystallography 🌐 English ⚖ 178 KB

The title compound, C 10 H 9 ClO 2 S, was prepared by the oxidation of 5-chloro-2-methyl-3-methylsulfanyl-1-benzofuran using 3-chloroperbenzoic acid. The benzofuran ring system is almost planar. Noor -CH 2 -HÁ Á Á interactions were observed.

5-Methyl-3-methylsulfinyl-2-phenyl-1-ben
✍ Choi, Hong Dae ;Seo, Pil Ja ;Son, Byeng Wha ;Lee, Uk 📂 Article 📅 2007 🏛 International Union of Crystallography 🌐 English ⚖ 752 KB

The title compound, C 16 H 14 O 2 S, was prepared by the oxidation of 3,5-dimethyl-2-phenyl-1-benzofuran using 3chloroperbenzoic acid. The O atom and the methyl group of the methylsulfinyl substituent lie on opposite sides of the plane of the benzofuran fragment. The phenyl ring is rotated out of th