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3339-79-5 (5-Iodo-2,2'-bithiophene,5-iodo-2,2'-bithiophene)

结构式：

5-Iodo-2,2'-bithiophene结构式图片|3339-79-5结构式图片

5-Iodo-2,2'-bithiopheneMOL文件

CAS号：

3339-79-5

中文名称：

5-Iodo-2,2'-bithiophene

英文名称：

5-iodo-2,2'-bithiophene

分子式：

C₈H₅IS₂

分子量：

292.159771680832

5-Iodo-2,2'-bithiophene(3339-79-5)名称与标识符

名称

中文别名：

5-Iodo-2,2'-bithiophene;

英文别名：

5-iodo-2,2'-bithiophene;5-Iodo-[2,2']bithiophene;5-Jod-1-amino-naphthalin;5-iodo-[1]naphthylamine;5-iodo-[2,2']bithiophenyl;5-iodonaphthalene-1-amine;5-iodo-2,2'-dithienyl;5-Jod-[1]naphthylamin;5-iodo-[2,2']-bithiophenyl;5-iodo-2,2'-bithienyl;1-Amino- 5-iodonaphthalene;5-Iodo-[2,2']bithiophene; 5-Jod-1-amino-naphthalin; 5-iodo-[1]naphthylamine; 5-iodo-[2,2']bithiophenyl; 5-iodonaphthalene-1-amine; 5-iodo-2,2'-dithienyl; 5-Jod-[1]naphthylamin; 5-iodo-[2,2']-bithiophenyl; 5-iodo-2,2'-bithienyl; 1-Amino- 5-iodonaphthalene;;2,2'-Bithiophene, 5-iodo-;

标识符

InChIKey：

XNKCDNYCFPPVAX-UHFFFAOYSA-N

Inchi：

1S/C8H5IS2/c9-8-4-3-7(11-8)6-2-1-5-10-6/h1-5H

SMILES：

C1(C2SC=CC=2)SC(I)=CC=1

5-Iodo-2,2'-bithiophene(3339-79-5)物化性质

实验特性

PSA : 0
沸点 : 75 °C(Press: 0.007 Torr)
熔点 : 31 °C
密度 : 1.875±0.06 g/cm3(Predicted)

计算特性

精确分子量 : 291.88735

5-Iodo-2,2'-bithiophene(3339-79-5)相关文献

1. Novel diphenylphosphine derivatives of 2,2′-bithiophene, 2,2′:5′,2″-terthiophene, 2-(2′-thienyl)pyridine and 2,6-di-2′-thienylpyridine. Crystal structures of 5,5′-bis(diphenylphosphino)-2,2′-bithiophene, diphenyl{5-[6′-(diphenylphosphino)-2′-pyridyl]-2-thienyl}phosphine and 2,6-bis[5′-(diphenylphosphino)-2′-thienyl]pyridine
John S. Field,Raymond J. Haines,Elena I. Lakoba,M. Hal Sosabowski J. Chem. Soc. Perkin Trans. 1 2001 3352
2. Dye-functionalized head-to-tail coupled oligo(3-hexylthiophenes)—perylene–oligothiophene dyads for photovoltaic applications
Jens Cremer,Elena Mena-Osteritz,Neil G. Pschierer,Klaus Müllen,Peter B?uerle Org. Biomol. Chem. 2005 3 985
3. New type of organic semiconductors for field-effect transistors with carbon-carbon triple bonds
Qing Meng,Jianhua Gao,Rongjin Li,Lang Jiang,Chengliang Wang,Huaping Zhao,Caiming Liu,Hongxiang Li,Wenping Hu J. Mater. Chem. 2009 19 1477
4. Synthesis and characterization of perylene–bithiophene–triphenylamine triads: studies on the effect of alkyl-substitution in p-type NiO based photocathodes
Martin Weidelener,Amaresh Mishra,Andrew Nattestad,Satvasheel Powar,Attila J. Mozer,Elena Mena-Osteritz,Yi-Bing Cheng,Udo Bach,Peter B?uerle J. Mater. Chem. 2012 22 7366
5. Synthesis and characterization of perylene–bithiophene–triphenylamine triads: studies on the effect of alkyl-substitution in p-type NiO based photocathodes
Martin Weidelener,Amaresh Mishra,Andrew Nattestad,Satvasheel Powar,Attila J. Mozer,Elena Mena-Osteritz,Yi-Bing Cheng,Udo Bach,Peter B?uerle J. Mater. Chem. 2012 22 7366
6. Highly enantioselective “inherently chiral” electroactive materials based on a 2,2′-biindole atropisomeric scaffold
Serena Arnaboldi,Tiziana Benincori,Andrea Penoni,Luca Vaghi,Roberto Cirilli,Sergio Abbate,Giovanna Longhi,Giuseppe Mazzeo,Sara Grecchi,Monica Panigati,Patrizia Romana Mussini Chem. Sci. 2019 10 2708
7. Molecular engineering of twisted dipolar chromophores for efficiency boosted BHJ solar cells
Abbasriyaludeen Abdul Raheem,Chitra Kumar,Ramasamy Shanmugam,P. Murugan,Chandrasekar Praveen J. Mater. Chem. C 2021 9 4562
8. Molecular engineering of twisted dipolar chromophores for efficiency boosted BHJ solar cells
Abbasriyaludeen Abdul Raheem,Chitra Kumar,Ramasamy Shanmugam,P. Murugan,Chandrasekar Praveen J. Mater. Chem. C 2021 9 4562
9. Diamond surface functionalization: from gemstone to photoelectrochemical applications
Jorne Raymakers,Ken Haenen,Wouter Maes J. Mater. Chem. C 2019 7 10134
10. Solution processable donor–acceptor oligothiophenes for bulk-heterojunction solar cells
Weifeng Zhang,Shing Chi Tse,Jianping Lu,Ye Tao,Man Shing Wong J. Mater. Chem. 2010 20 2182

目录

相关化合物

104499-99-2(2,5-bis(5-iodothiophen-2-yl)thiophene) 792913-82-7((8-甲基-1,4-二氧杂螺[4.5]癸烷-8-基)氨基甲酸叔丁酯) 79324-78-0(1-(3-溴-4-(甲基硫代)苯基)乙酮) 78861-31-1(1,4-丁二醇，1-（4-甲基苯基）-) 78930-16-2(4-羟基-4-苯氧基苯甲酮) 78946-25-5(3-溴-4-(溴甲基)苯甲酸甲酯) 79456-27-2(6-氯-3-(三氟甲基)吡啶-2-胺) 795310-80-4(4-(3-甲基-1,2,4-氧杂二唑-5-基)哌啶盐酸盐)

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