Weight | 128.171 g/mol |
---|---|
Formula | C7H12O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 1 |
Methyl cyclopentanecarboxylate (4630-80-2)
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- Scalable Synthesis and Isolation of the Four Stereoisomers of Methyl 1-Amino-3-(4-bromophenyl)cyclopentanecarboxylate, Useful Intermediates for the Synthesis of S1P1 Receptor Agonists (Journal of Organic Chemistry, 2009)
- ChemInform Abstract: Enantioselective Hydrolysis of Dimethyl 2,3-((Dimethylmethylene)dioxy)-5-hydroxy-1,4-cy# clopentanedicarboxylate with Pig Liver Esterase. Stereoselective Synthesis of Methyl 2(R),3(S)-((Dimethylmethylene)dioxy)-5(R)-hydroxy-1(S)-carboxy-4(R)-cyclopentanecarboxylate. A Cyclopentane Synthone with All Ring Atoms Chiral. (ChemInform, 1988)
- Reaction of Methyl 1-(2-Bromoisobutyryl)cyclopentanecarboxylate and 3-(1-Bromocyclopentyl)-2,2-dimethyl-3-oxopropionate with Zinc and Aromatic Aldehydes. (ChemInform, 2004)
- Synthesis of Methyl Cyclopentanecarboxylate: A Laboratory Experience in Carbon Rearrangement (Journal of Chemical Education, 2016)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC(=O)C1CCCC1
-
InChIKeyIIHIJFJSXPDTNO-UHFFFAOYSA-N
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