220884
2-Thiophenemethylamine
96%
Sinonimo/i:
2-(Aminomethyl)thiophene
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About This Item
Formula empirica (notazione di Hill):
C5H7NS
Numero CAS:
Peso molecolare:
113.18
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Livello qualitativo
Saggio
96%
Stato
liquid
liquid
Indice di rifrazione
n20/D 1.5670 (lit.)
P. ebollizione
95-99 °C/28 mmHg (lit.)
Densità
1.103 g/mL at 25 °C (lit.)
Gruppo funzionale
amine
Stringa SMILE
NCc1cccs1
InChI
1S/C5H7NS/c6-4-5-2-1-3-7-5/h1-3H,4,6H2
FKKJJPMGAWGYPN-UHFFFAOYSA-N
Categorie correlate
Descrizione generale
2-Thiophenemethylamine is a potential ligand replacement for poly(3-hexylthiophene)/CdSe hybrid solar cells.
Applicazioni
2-Thiophenemethylamine was used in preparation of:
- naphthalene-thiophene hybrid molecule (Z)-1-((thiophen-2-ylmethylamino)methylene)naphthalen-2(1H)-one
- fluorescent Pd2+ sensor, N-butyl-4-(p-methyloxy)-phenylethynyl-5-thiophenemethylamino-1,8-naphthalimide
Reactant involved in synthesis of:
Reactant involved in:
- Triazole-linked-thiopene conjugates for use as a biomimetic model for studies of metal detoxification and oxidative stress involving metallothionein
- Serotonin 5-HT1A receptor antagonists which have neuroprotective affects against ischemic cell damage
- Imidazole- and piperonyl-containing thiadiazoles and pyrimidines for use as inducible oxide synthase dimerization inhibitors
- Optoelectronic segmented polyurethanes
Reactant involved in:
- Studies of organocatalyzed asymmetric reductive amination of ketones
- Metal-free aerobic oxidative coupling of amines to imines
Avvertenze
Danger
Indicazioni di pericolo
Classi di pericolo
Skin Corr. 1B
Codice della classe di stoccaggio
8A - Combustible corrosive hazardous materials
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
165.2 °F - closed cup
Punto d’infiammabilità (°C)
74 °C - closed cup
Dispositivi di protezione individuale
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Debasis Karak et al.
Dalton transactions (Cambridge, England : 2003), 42(19), 6708-6715 (2013-04-10)
A naphthalene-thiophene hybrid molecule (Z)-1-((thiophen-2-ylmethylamino)methylene)naphthalen-2(1H)-one () was prepared by condensation of 2-thiophenemethylamine and 2-hydroxy-1-naphthaldehyde. According to FTIR, (1)H NMR spectrometry and single crystal X-ray analysis, exists in the cis-keto-amine tautomeric form. behaves like a molecular AND type binary logic gate
Liping Duan et al.
Chemical communications (Cambridge, England), (47)(47), 6339-6341 (2008-12-03)
A new fluorescent Pd2+ sensor , N-butyl-4-(p-methyloxy)-phenylethynyl-5-thiophenemethylamino-1,8-naphthalimide, was designed and synthesized. It showed highly selective on-off fluorescence changes for Pd2+ among the representative transition and heavy metallic cations, and its fluorescence was efficiently quenched by 5 equivalents of Pd2+ in
Jun Yan Lek et al.
ACS applied materials & interfaces, 3(2), 287-292 (2011-01-26)
For hybrid solar cells, interfacial chemistry is one of the most critical factors for good device performance. We have demonstrated that the size of the surface ligands and the dispersion of nanoparticles in the solvent and in the polymer are
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 220884-5G | 4061838776709 |
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