682500
Copper(I) thiophene-2-carboxylate
Sinonimo/i:
Cu (TC)
Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
About This Item
Formula empirica (notazione di Hill):
C5H3CuO2S
Numero CAS:
Peso molecolare:
190.69
Numero MDL:
Codice UNSPSC:
12161600
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
![(R)-1-[(SP)-2-(Diphenylphosphino)ferrocenyl]ethyldicyclohexylphosphine ≥97%](/deepweb/assets/sigmaaldrich/product/structures/245/493/2ae2dd8a-65cc-4aba-9a1f-1292eb1ad8e0/640/2ae2dd8a-65cc-4aba-9a1f-1292eb1ad8e0.png)
Forma fisica
solid
Livello qualitativo
Impiego in reazioni chimiche
core: copper
reaction type: C-C Bond Formation
reagent type: catalyst
Stringa SMILE
[Cu]OC(=O)c1cccs1
InChI
1S/C5H4O2S.Cu/c6-5(7)4-2-1-3-8-4;/h1-3H,(H,6,7);/q;+1/p-1
SFJMFSWCBVEHBA-UHFFFAOYSA-M
Applicazioni
Copper(I) thiophene-2-carboxylate can be used as a reactant or reagent in:
- Studies of xenobiotic response to herbicide safener derivatives.
- Synthesis of functionalized BODIPY dye analogs.
- Orthogonal cross-coupling reactions.
- Preparation of parent borondipyrromethene system.
- Copper mediated cross-coupling.
Reactant or reagent involved in:
- Studies of xenobiotic response to herbicide safener derivatives
- Synthesis of functionalized BODIPY dye analogs
- Orthogonal cross-coupling reactions
- Preparation of parent borondipyrromethene system
- Copper mediated cross-coupling
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Aquatic Acute 1 - Aquatic Chronic 1
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Scegli una delle versioni più recenti:
Possiedi già questo prodotto?
I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.
I clienti hanno visto anche
![[Ir(dF(Me)ppy)2(dtbbpy)]PF6](/deepweb/assets/sigmaaldrich/product/structures/150/099/7c2dfa31-39f4-4cca-aee5-86d4a89fea78/640/7c2dfa31-39f4-4cca-aee5-86d4a89fea78.png)
Xenobiotic responsiveness of Arabidopsis thaliana to a chemical series derived from a herbicide safener.
Skipsey M, et al.
The Journal of Biological Chemistry, 286(37), 32268-32276 (2011)
The smallest and one of the brightest. Efficient preparation and optical description of the parent borondipyrromethene system.
Arroyo I J, et al.
The Journal of Organic Chemistry, 74(15), 5719-5722 (2009)
Regioselective Syntheses of 2, 3?Substituted Pyridines by Orthogonal Cross?Coupling Strategies.
Koley M, et al.
European Journal of Organic Chemistry, 2011(10), 1972-1979 (2011)
2?and 3?Monohalogenated BODIPY Dyes and Their Functionalized Analogues: Synthesis and Spectroscopy.
Leen V, et al.
European Journal of Organic Chemistry, 2011(23), 4386-4396 (2011)
N-Amidation by copper-mediated cross-coupling of organostannanes or boronic acids with O-acetyl hydroxamic acids.
Zhang Z, et al.
Organic Letters, 10(14), 3005-3008 (2008)
Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..
Contatta l'Assistenza Tecnica.