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2,3,3-Trimethylindolenine | CAS:1640-39-7
2,3,3-Trimethylindolenine
  • Name:2,3,3-Trimethylindolenine
  • CAS:1640-39-7
  • Synonyms:2,3,3-Trimethyl-3H-indole
  • Molecular Formula:C11H13N
  • Molecular Weight:159.23
  • EINESC:216-685-6

Description

Properties

Boiling point 228-229 ºC (744 mmHg)
Flash point 93 ºC
Density 0.992
Refractive index 1.545

Safety

Symbol(GHS) Xi
Hazard Codes R36/37/38
SDS/MSDS S26;S37/39

SDS

Source SDS/MSDS Samples
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Articles
Peer-Reviewed Papers
Thiophene-benzoquinones: synthesis, crystal structures and preliminary coordination chemistry of derived anilate ligands.Matteo Atzori et al.Organic & biomolecular chemistry, 12(43), 8752-8763 (2014-09-30) Microwave assisted synthesis, experimental and theoretical characterization and antibacterial activity screening of novel azomethine compounds containing thiophene and aminophenol functionality.Emel Ermiş et al.Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 243, 118761-118761 (2020-08-28) Microwave synthesis and fluorous purification of 4-(tetrathienyl) butyric acid for self-assembled monolayer semiconductor applications.McCairn MC, et al. Tetrahedron Letters, 49(8), 1328-1330 (2008) Effect of the acceptor moiety on the electrochemical and electrochromic properties of Donor-Acceptor-Donor polymer films.Triantou D, et al. International Journal of Electrochemical Science, 10, 3458-3477 (2015) A Comparison of ACQ, AIE and AEE-Based Polymers Loaded on Polyurethane Foams as Sensors for Explosives Detection.Zhiwei Chu et al.Sensors (Basel, Switzerland), 18(5) (2018-05-16) Synthesis, emission and spectro-electrochemical studies of bithienylnaphthalene systems.Sankaran B, et al. Synthetic Metals, 123(3), 425-433 (2001) Two-dimensional structural motif in thienoacene semiconductors: Synthesis, structure, and properties of tetrathienoanthracene isomers.Brusso JL, et al. Chemistry of Materials, 20(7), 2484-2494 (2008) Phenoxazine based units--synthesis, photophysics and electrochemistry.Anna Nowakowska-Oleksy et al.Journal of fluorescence, 21(1), 169-178 (2010-07-14)
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