395137
2-(Trichloroacetyl)pyrrole
99%
Synonym(s):
2-Pyrrolyl trichloromethyl ketone
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About This Item
Empirical Formula (Hill Notation):
C6H4Cl3NO
CAS Number:
Molecular Weight:
212.46
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
99%
mp
72-74 °C (lit.)
functional group
chloro
ketone
SMILES string
ClC(Cl)(Cl)C(=O)c1ccc[nH]1
InChI
1S/C6H4Cl3NO/c7-6(8,9)5(11)4-2-1-3-10-4/h1-3,10H
InChI key
BBFDGMDENAEMKF-UHFFFAOYSA-N
General description
2-(Trichloroacetyl)pyrrole is a 2-substituted pyrrole. It undergoes acylation to afford 4-acyl derivatives (4-formyl to 4-hexanoyl).
Application
2-(Trichloroacetyl)pyrrole may be used in the synthesis of following:
- pyrrole-2-carboxylates, tris[2-(2-pyrryl-carboxy)ethyl]amine and tetrakis(2-pyrryl-carboxy-methyl)methane
- 1-oxo-2,3-disubstituted -pyrrolo[1,2-a]pyrazines
- 4-pyridylmethyl 1H-pyrrole-2-carboxylate
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Find documentation for the products that you have recently purchased in the Document Library.
Total synthesis of peramine.
Dumas, DJ.
The Journal of Organic Chemistry, 53(20), 4650-4653 (1988)
4-Pyridylmethyl 1H-pyrrole-2-carboxylate.
Wang W-Y and Yin Z-M.
Acta Crystallographica Section E, Structure Reports Online, 63(5), o2737-o2738 (2007)
Synthesis of 2-alkylputrescines from 3-alkylpyrroles.
Garrido DOA, et al.
The Journal of Organic Chemistry, 53(2), 403-407 (1988)
Pyrrole-2-carboxylate dimer: a robust supramolecular synthon for crystal engineering.
Yin Z and Li Z.
Tetrahedron Letters, 47(45), 7875-7879 (2006)
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