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Revision as of 15:03, 30 November 2010 editCheMoBot (talk | contribs)Bots141,565 edits Updating {{chembox}} (no changed fields - added verified revid - updated 'UNII_Ref', 'ChemSpiderID_Ref', 'StdInChI_Ref', 'StdInChIKey_Ref') per Chem/Drugbox validation (report [[Wikipedia_talk:Wi← Previous edit Latest revision as of 09:31, 16 February 2022 edit undoM97uzivatel (talk | contribs)Extended confirmed users6,558 editsNo edit summary 
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{{Redirect|CuTC||CUTC (disambiguation)}} {{Redirect|CuTC||CUTC (disambiguation)}}
{{Chembox {{Chembox
|Watchedfields = changed
| verifiedrevid = 399729557 |verifiedrevid = 399731183
| Reference = <ref> at ]</ref> |Reference = <ref> at ]</ref>
| ImageFile = Copper(I)-thiophene-2-carboxylate.png |ImageFile = Copper(I)-thiophene-2-carboxylate.png
| ImageSize = 150px |ImageSize = 150px
| IUPACName = Copper(I) thiophene-2-carboxylate |IUPACName = Copper(I) thiophene-2-carboxylate
| OtherNames = CuTC |OtherNames = CuTC
| Section1 = {{Chembox Identifiers |Section1={{Chembox Identifiers
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 9369899 |ChemSpiderID = 9369899
| InChI = 1/C5H4O2S.Cu/c6-5(7)4-2-1-3-8-4;/h1-3H,(H,6,7);/q;+1/p-1 |InChI = 1/C5H4O2S.Cu/c6-5(7)4-2-1-3-8-4;/h1-3H,(H,6,7);/q;+1/p-1
| InChIKey = SFJMFSWCBVEHBA-REWHXWOFAY |InChIKey = SFJMFSWCBVEHBA-REWHXWOFAY
| SMILES1 = .C(=O)c1sccc1 |SMILES1 = .C(=O)c1sccc1
| StdInChI_Ref = {{stdinchicite|correct|chemspider}} |StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/C5H4O2S.Cu/c6-5(7)4-2-1-3-8-4;/h1-3H,(H,6,7);/q;+1/p-1 |StdInChI = 1S/C5H4O2S.Cu/c6-5(7)4-2-1-3-8-4;/h1-3H,(H,6,7);/q;+1/p-1
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = SFJMFSWCBVEHBA-UHFFFAOYSA-M |StdInChIKey = SFJMFSWCBVEHBA-UHFFFAOYSA-M
| CASNo = 68986-76-5
|CASNo_Ref = {{cascite|correct|??}}
| PubChem = 11194830
|CASNo = 68986-76-5
| SMILES = O=C()C1=CC=CS1.
|UNII_Ref = {{fdacite|correct|FDA}}
|UNII = 7519WBL07L
|PubChem = 11194830
|EINECS = 633-277-7
|SMILES = O=C()C1=CC=CS1.
}} }}
| Section2 = {{Chembox Properties |Section2={{Chembox Properties
| C=5|H=3|Cu=1|O=2|S=1 | C=5 | H=3 | Cu=1 | O=2 | S=1
}}
| Appearance =
|Section3={{Chembox Hazards
| Density =
|MainHazards = Irritant
| MeltingPt =
|GHSPictograms = {{GHS07}}
| BoilingPt =
|GHSSignalWord = Warning
| Solubility = }}
|HPhrases = {{H-phrases|315|319|335}}
| Section3 = {{Chembox Hazards
|PPhrases = {{P-phrases|261|264|271|280|302+352|304+340|305+351+338|312|321|332+313|337+313|362|403+233|405|501}}
| MainHazards = Irritant ('''Xi''')
|PEL = TWA 1 mg/m<sup>3</sup> (as Cu)<ref name=PGCH>{{PGCH|0150}}</ref>
| RPhrases = {{R36/37/38}}
|REL = TWA 1 mg/m<sup>3</sup> (as Cu)<ref name=PGCH/>
| SPhrases = {{S26}}
|IDLH = TWA 100 mg/m<sup>3</sup> (as Cu)<ref name=PGCH/>}}
| FlashPt =
| Autoignition = }}
}} }}


'''Copper(I)-thiophene-2-carboxylate''' or '''CuTC''' is a ] and a ] in ] that especially promotes the ] between ] ]s.<ref>{{cite journal | doi = 10.1021/cr000664r | title = Aryl-Aryl Bond Formation One Century after the Discovery of the Ullmann Reaction | author = Jwanro Hassan, Marc Sévignon, Christel Gozzi, Emmanuelle Schulz, and Marc Lemaire | journal = Chem. Rev. | year = 2002 | volume = 102 | issue = 5 | pages = 1359–1470 | url = http://pubs.acs.org/spotlight/july2002/cr000664r.pdf | pmid = 11996540}}</ref> '''Copper(I) thiophene-2-carboxylate''' or '''CuTC''' is a ] derived from copper and ]. It is used as a ] to promote the ] between ] ]s.<ref>{{cite journal | doi = 10.1021/jo9700078 | title = Ambient Temperature, Ullmann-like Reductive Coupling of Aryl, Heteroaryl, and Alkenyl Halides |author1=Shijie Zhang |author2=Dawei Zhang |author3=Lanny S. Liebeskind | journal = J. Org. Chem. | year = 1997 | volume = 62 | issue = 8 | pages = 2312–2313 | pmid = 11671553}}</ref>


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== References == == References ==
{{reflist}} {{reflist}}


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