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2-Thiophenmethylamin
96%
Synonym(e):
2-(Aminomethyl)-thiophen
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About This Item
Empirische Formel (Hill-System):
C5H7NS
CAS-Nummer:
Molekulargewicht:
113.18
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
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Qualitätsniveau
Assay
96%
Form
liquid
liquid
Brechungsindex
n20/D 1.5670 (lit.)
bp
95-99 °C/28 mmHg (lit.)
Dichte
1.103 g/mL at 25 °C (lit.)
Funktionelle Gruppe
amine
SMILES String
NCc1cccs1
InChI
1S/C5H7NS/c6-4-5-2-1-3-7-5/h1-3H,4,6H2
InChIKey
FKKJJPMGAWGYPN-UHFFFAOYSA-N
Verwandte Kategorien
Allgemeine Beschreibung
2-Thiophenemethylamine is a potential ligand replacement for poly(3-hexylthiophene)/CdSe hybrid solar cells.
Anwendung
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
Signalwort
Danger
H-Sätze
Gefahreneinstufungen
Skin Corr. 1B
Lagerklassenschlüssel
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flammpunkt (°F)
165.2 °F - closed cup
Flammpunkt (°C)
74 °C - closed cup
Persönliche Schutzausrüstung
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
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