Category: 474416-61-0

Brzezinski, Jacek Z. et al. published their research in Synthesis in 2002 | CAS: 474416-61-0

Bis(2-iodothiophen-3-yl)methanone (cas: 474416-61-0) belongs to iodide derivatives. Typical reactions of alkyl iodides include nucleophilic substitution, elimination, reduction, and the formation of organometallics. Iodo alkanes participate in a variety of organic synthesis reactions, which include the Simmons鑱砈mith reaction (cyclopropanation using iodomethane), Williamson ether synthesis, Wittig reaction, Grignard reaction, alkyl coupling reactions, and Wurtz reaction.Reference of 474416-61-0

A new, improved and convenient synthesis of 4H-cyclopenta[2,1-b:3,4-b’]-dithiophen-4-one was written by Brzezinski, Jacek Z.;Reynolds, John R.. And the article was included in Synthesis in 2002.Reference of 474416-61-0 This article mentions the following:

A new and efficient three-step synthesis of 4H-cyclopenta[2,1-b:3,4-b’]dithiophen-4-one is described. This was achieved by a one-pot, regiospecific synthesis of bis(2-iodo-3-thienyl)methanol, its subsequent oxidation to the bis(2-iodo-3-thienyl) ketone which after Ullmann coupling yielded the title compound In the experiment, the researchers used many compounds, for example, Bis(2-iodothiophen-3-yl)methanone (cas: 474416-61-0Reference of 474416-61-0).

Bis(2-iodothiophen-3-yl)methanone (cas: 474416-61-0) belongs to iodide derivatives. Typical reactions of alkyl iodides include nucleophilic substitution, elimination, reduction, and the formation of organometallics. Iodo alkanes participate in a variety of organic synthesis reactions, which include the Simmons鑱砈mith reaction (cyclopropanation using iodomethane), Williamson ether synthesis, Wittig reaction, Grignard reaction, alkyl coupling reactions, and Wurtz reaction.Reference of 474416-61-0

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Brzezinski, Jacek Z. et al. published their research in Synthesis in 2002 | CAS: 474416-61-0

Bis(2-iodothiophen-3-yl)methanone (cas: 474416-61-0) belongs to iodide derivatives. Typical reactions of alkyl iodides include nucleophilic substitution, elimination, reduction, and the formation of organometallics. Iodo alkanes participate in a variety of organic synthesis reactions, which include the Simmons–Smith reaction (cyclopropanation using iodomethane), Williamson ether synthesis, Wittig reaction, Grignard reaction, alkyl coupling reactions, and Wurtz reaction.Reference of 474416-61-0

A new, improved and convenient synthesis of 4H-cyclopenta[2,1-b:3,4-b’]-dithiophen-4-one was written by Brzezinski, Jacek Z.;Reynolds, John R.. And the article was included in Synthesis in 2002.Reference of 474416-61-0 This article mentions the following:

A new and efficient three-step synthesis of 4H-cyclopenta[2,1-b:3,4-b’]dithiophen-4-one is described. This was achieved by a one-pot, regiospecific synthesis of bis(2-iodo-3-thienyl)methanol, its subsequent oxidation to the bis(2-iodo-3-thienyl) ketone which after Ullmann coupling yielded the title compound In the experiment, the researchers used many compounds, for example, Bis(2-iodothiophen-3-yl)methanone (cas: 474416-61-0Reference of 474416-61-0).

Bis(2-iodothiophen-3-yl)methanone (cas: 474416-61-0) belongs to iodide derivatives. Typical reactions of alkyl iodides include nucleophilic substitution, elimination, reduction, and the formation of organometallics. Iodo alkanes participate in a variety of organic synthesis reactions, which include the Simmons–Smith reaction (cyclopropanation using iodomethane), Williamson ether synthesis, Wittig reaction, Grignard reaction, alkyl coupling reactions, and Wurtz reaction.Reference of 474416-61-0

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Sutter, Alexandra et al. published their research in Synlett in 2014 | CAS: 474416-61-0

Bis(2-iodothiophen-3-yl)methanone (cas: 474416-61-0) belongs to iodide derivatives. Organoiodine compounds occur widely in organic chemistry, but are relatively rare in nature. Iodo alkanes participate in a variety of organic synthesis reactions, which include the Simmons–Smith reaction (cyclopropanation using iodomethane), Williamson ether synthesis, Wittig reaction, Grignard reaction, alkyl coupling reactions, and Wurtz reaction.Related Products of 474416-61-0

A versatile synthesis of long-wavelength-excitable BODIPY dyes from readily modifiable cyclopenta[2,1-b:3,4-b’]dithiophenes was written by Sutter, Alexandra;Ziessel, Raymond. And the article was included in Synlett in 2014.Related Products of 474416-61-0 This article mentions the following:

Knoevenagel condensation of a simple methylated borondipyrromethene (Bodipy) with 4,4′-dihexyl-4H-cyclopenta-[2,1-b:3,4-b’]dithiophenes functionalized at one end by a triphenylamine residue and at the other by a carbaldehyde fragment leads to novel dye species. These bisvinylic derivatives exhibit pronounced absorption in the visible range extending above 850 nm. Addition of other Bodipy units by coupling to a central iodophenyl entity enables filling of the gaps in absorption of the pivotal starting material. Efficient cascade energy transfer between the Bodipys is facilitated by spectral overlap between the energy donor and the energy acceptor. All photons between 350 nm and 750 nm are channeled to the distyryl centers which emit at 864 nm. In the experiment, the researchers used many compounds, for example, Bis(2-iodothiophen-3-yl)methanone (cas: 474416-61-0Related Products of 474416-61-0).

Bis(2-iodothiophen-3-yl)methanone (cas: 474416-61-0) belongs to iodide derivatives. Organoiodine compounds occur widely in organic chemistry, but are relatively rare in nature. Iodo alkanes participate in a variety of organic synthesis reactions, which include the Simmons–Smith reaction (cyclopropanation using iodomethane), Williamson ether synthesis, Wittig reaction, Grignard reaction, alkyl coupling reactions, and Wurtz reaction.Related Products of 474416-61-0

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com