Weight | 125.127 g/mol |
---|---|
Formula | C6H7NO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
Methyl 1H-pyrrole-2-carboxylate (1193-62-0)
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- Discovery and synthesis of methyl 2,5-dimethyl-4-[2- (phenylmethyl)benzoyl]-1H-pyrrole-3-carboxylate (FPL 64176) and analogues: the first examples of a new class of calcium channel activator. (Journal of Medicinal Chemistry, 1993)
- Efficient syntheses of ethyl 4-cyano-5-hydroxy-2-methyl-1H-pyrrole-3-carboxylate and ethyl (2Z)-(4-cyano-5-oxopyrrolidin-2-ylidene)ethanoate (Tetrahedron Letters, 2011)
- Five-membred 2,3-dioxoheterocycles: LXXXI. Reactions of 4,5-bis(methoxycarbonyl)-1H-pyrrole-2,3-diones with N-substituted 3-amino-5,5-dimethyl-2-cyclohex-2-en-1-ones. crystal and molecular structure of methyl 4-hydroxy-6,6-dimethyl-1,1-bis(4-methylphenyl)-2,4,5-trioxo-1,1,2,4,5,5,6,7-octahydrospiro[indole-3,2-pyrrole]-3-carboxylate (Russian Journal of Organic Chemistry, 2011)
- Methyl 4-p-tolyl-1H-pyrrole-2-carboxylate (Acta Crystallographica Section E: Crystallographic Communications, 2007)
- Selective Formation of Pyrrolo[3,2-d]pyrimidines from Methyl[(N-benzoyl-S-methylisothiocarbamoyl)amino]-1H-pyrrole-2-carboxylate (Organic Process Research & Development, 2000)
- ChemInform Abstract: Azoalkene Route to Methyl 2,5Dimethyl4(2(phenylmethyl)benzoyl)1H pyrrole3carboxylate (FPL 64176) and Analogues: Synthesis of 1(Boc Amino)pyrrole3carboxylates and Their Conversion to 1HPyrroles via 1 Aminopyrroles. (Synthesis, 1994)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC(=O)C1=CC=CN1
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InChIKeyVONGYFFEWFJHNP-UHFFFAOYSA-N
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