3-Thiophene acetic acid References Navigation menu6964-21-221886100.027.424verify10.1038/nature13892expanding ite

ThiophenesAcetic acidsOrganic compound stubs


organosulfur compoundpolythiophene























3-Thiophene acetic acid

3-taa.png
Names
Other names
3-TAA, Thiophen-3-yl-acetic acid

Identifiers

CAS Number


  • 6964-21-2


ChemSpider


  • 21886 ☑Y


ECHA InfoCard

100.027.424


Properties

Chemical formula

C6H6O2S

Molar mass
142.18 g/mol
Appearance
colorless or white solid

Density
1.336 g/cm3

Melting point
 79–80 °C (174–176 °F; 352–353 K)

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).


☑Y verify (what is ☑Y☒N ?)

Infobox references


3-Thiophene acetic acid is an organosulfur compound with the formula HO2CCH2C4H3S. It is a white solid. The compound has attracted attention as a precursor to functionalized derivatives of polythiophene.[1]



References



  1. ^ Huo, Haohua; Shen, Xiaodong; Wang, Chuanyong; Zhang, Lilu; Roese, Philipp; Chen, Liang-An; Harms, Klaus; Marsch, Michael; Hilt, Gerhard; Meggers, Eric (2014). "Asymmetric photoredox transition-metal catalysis activated by visible light". Nature. 515: 100–103. doi:10.1038/nature13892.CS1 maint: Uses authors parameter (link).mw-parser-output cite.citationfont-style:inherit.mw-parser-output .citation qquotes:"""""""'""'".mw-parser-output .citation .cs1-lock-free abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Lock-green.svg/9px-Lock-green.svg.png")no-repeat;background-position:right .1em center.mw-parser-output .citation .cs1-lock-limited a,.mw-parser-output .citation .cs1-lock-registration abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/Lock-gray-alt-2.svg/9px-Lock-gray-alt-2.svg.png")no-repeat;background-position:right .1em center.mw-parser-output .citation .cs1-lock-subscription abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/a/aa/Lock-red-alt-2.svg/9px-Lock-red-alt-2.svg.png")no-repeat;background-position:right .1em center.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registrationcolor:#555.mw-parser-output .cs1-subscription span,.mw-parser-output .cs1-registration spanborder-bottom:1px dotted;cursor:help.mw-parser-output .cs1-ws-icon abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/4/4c/Wikisource-logo.svg/12px-Wikisource-logo.svg.png")no-repeat;background-position:right .1em center.mw-parser-output code.cs1-codecolor:inherit;background:inherit;border:inherit;padding:inherit.mw-parser-output .cs1-hidden-errordisplay:none;font-size:100%.mw-parser-output .cs1-visible-errorfont-size:100%.mw-parser-output .cs1-maintdisplay:none;color:#33aa33;margin-left:0.3em.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration,.mw-parser-output .cs1-formatfont-size:95%.mw-parser-output .cs1-kern-left,.mw-parser-output .cs1-kern-wl-leftpadding-left:0.2em.mw-parser-output .cs1-kern-right,.mw-parser-output .cs1-kern-wl-rightpadding-right:0.2em







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