Revision as of 07:28, 28 September 2011 editحسن علي البط (talk | contribs)Extended confirmed users, Pending changes reviewers19,940 edits removed Category:Carboxylic acids; added Category:Acetic acids using HotCat← Previous edit | Latest revision as of 13:15, 9 January 2022 edit undoSmokefoot (talk | contribs)Autopatrolled, Extended confirmed users, Pending changes reviewers, Rollbackers75,055 edits rename | ||
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{{Orphan|date=December 2008}} | |||
{{Chemical-importance|date=September 2010}} | |||
{{chembox | {{chembox | ||
| verifiedrevid = |
| verifiedrevid = 477220217 | ||
| ImageFile = 3- |
| ImageFile = 3-Thiophene acetic acid.svg | ||
| ImageSize = | | ImageSize = | ||
| PIN = (Thiophen-3-yl)acetic acid | |||
| IUPACName = | |||
| OtherNames = 3-TAA, Thiophen-3-yl-acetic acid | | OtherNames = 3-TAA, Thiophen-3-yl-acetic acid | ||
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|Section1={{Chembox Identifiers | ||
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| CASNo = 6964-21-2 | ||
| CASNo_Ref = {{cascite|correct|CAS}} | |||
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| EC_number = 230-166-1 | |||
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| UNII_Ref = {{fdacite|correct|FDA}} | |||
| UNII = 3B235D2C4J | |||
⚫ | | PubChem = 23404 | ||
⚫ | | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ||
| ChemSpiderID = 21886 | | ChemSpiderID = 21886 | ||
| StdInChI_Ref = {{stdinchicite|correct|chemspider}} | | StdInChI_Ref = {{stdinchicite|correct|chemspider}} | ||
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | ||
| StdInChIKey = RCNOGGGBSSVMAS-UHFFFAOYSA-N | | StdInChIKey = RCNOGGGBSSVMAS-UHFFFAOYSA-N | ||
| SMILES = | | SMILES = C1=CSC=C1CC(=O)O | ||
}} | }} | ||
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|Section2={{Chembox Properties | ||
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| Formula = C<sub>6</sub>H<sub>6</sub>O<sub>2</sub>S | ||
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| MolarMass = 142.18 g/mol | ||
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| Appearance = colorless or white solid | ||
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| Density = 1.336 g/cm<sup>3</sup> | ||
| MeltingPtC =79-80 | |||
| MeltingPt = | |||
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| BoilingPt = | ||
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| Solubility = | ||
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|Section3={{Chembox Hazards | ||
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}} | }} | ||
'''Thiophene-3-acetic acid''' is an ] with the formula HO<sub>2</sub>CCH<sub>2</sub>C<sub>4</sub>H<sub>3</sub>S. It is a white solid. It is one of two isomers of thiophene acetic acid, the other being ]. | |||
'''3-Thiophene acetic acid''' is an ]. | |||
Thiophene-3-acetic acid has attracted attention as a precursor to functionalized derivatives of ].<ref>{{cite journal|title=Asymmetric photoredox transition-metal catalysis activated by visible light|author1=Huo, Haohua |author2=Shen, Xiaodong |author3=Wang, Chuanyong |author4=Zhang, Lilu |author5=Roese, Philipp |author6=Chen, Liang-An |author7=Harms, Klaus |author8=Marsch, Michael |author9=Hilt, Gerhard |author10=Meggers, Eric |display-authors=3|journal=Nature|year=2014|volume=515|issue=7525 |pages=100–103|doi=10.1038/nature13892|pmid=25373679 |bibcode=2014Natur.515..100H |s2cid=4456239 }}</ref> | |||
==References== | |||
<references /> | |||
{{DEFAULTSORT:Thiophene Acetic Acid, 3-}} | {{DEFAULTSORT:Thiophene Acetic Acid, 3-}} | ||
] | ] | ||
] | ] | ||
{{organic-compound-stub}} |
Latest revision as of 13:15, 9 January 2022
Names | |
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Preferred IUPAC name (Thiophen-3-yl)acetic acid | |
Other names 3-TAA, Thiophen-3-yl-acetic acid | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ChemSpider | |
ECHA InfoCard | 100.027.424 |
EC Number |
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PubChem CID | |
UNII | |
CompTox Dashboard (EPA) | |
InChI
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SMILES
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Properties | |
Chemical formula | C6H6O2S |
Molar mass | 142.18 g/mol |
Appearance | colorless or white solid |
Density | 1.336 g/cm |
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 , 100 kPa). Y verify (what is ?) Infobox references |
Thiophene-3-acetic acid is an organosulfur compound with the formula HO2CCH2C4H3S. It is a white solid. It is one of two isomers of thiophene acetic acid, the other being thiophene-2-acetic acid.
Thiophene-3-acetic acid has attracted attention as a precursor to functionalized derivatives of polythiophene.
References
- Huo, Haohua; Shen, Xiaodong; Wang, Chuanyong; et al. (2014). "Asymmetric photoredox transition-metal catalysis activated by visible light". Nature. 515 (7525): 100–103. Bibcode:2014Natur.515..100H. doi:10.1038/nature13892. PMID 25373679. S2CID 4456239.
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