288985
2-Thiophenecarbonyl chloride
97%
Synonym(s):
α-Thenoyl chloride
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About This Item
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Quality Level
Assay
97%
form
liquid
refractive index
n20/D 1.590 (lit.)
bp
206-208 °C (lit.)
density
1.371 g/mL at 25 °C (lit.)
functional group
acyl chloride
storage temp.
2-8°C
SMILES string
ClC(=O)c1cccs1
InChI
1S/C5H3ClOS/c6-5(7)4-2-1-3-8-4/h1-3H
InChI key
QIQITDHWZYEEPA-UHFFFAOYSA-N
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General description
The postfunctionalization reaction of 2-thiophenecarbonyl chloride with single walled carbon nanotubes (SWCNTs) was studied.
Application
2-Thiophenecarbonyl chloride was used in the synthesis of building blocks derived from ornithine by undergoing acylation/sulphonation of copper complex of orthinine.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
194.0 °F
Flash Point(C)
90 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Journal of the American Chemical Society, 135(49), 18385-18395 (2013-11-22)
The reactivity of reduced single walled carbon nanotubes (SWCNTs) (carbon nanotubides), prepared under strict inert conditions in a glovebox with respect to the covalent functionalization with hexyl iodide and subsequent exposure to ambient conditions (air, moisture), was systematically investigated by
The journal of peptide research : official journal of the American Peptide Society, 49(2), 183-189 (1997-02-01)
Recently great interest has arisen in the synthesis of combinatorial libraries, and this technology provides a significant partner to contemporary strategies in rational design and lead discovery. By simple combination of a given set of building blocks, high numbers of
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