Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H6O2 |
| Molecular Weight | 86.0892 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1CC1
InChI
InChIKey=YMGUBTXCNDTFJI-UHFFFAOYSA-N
InChI=1S/C4H6O2/c5-4(6)3-1-2-3/h3H,1-2H2,(H,5,6)
| Molecular Formula | C4H6O2 |
| Molecular Weight | 86.0892 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| 3-[(E)-2-Chloro-3,3,3-trifluoro-prop-1-en-1-yl]-N-(2-chloro-phen-yl)-2,2-dimethyl-cyclo-propane-1-carboxamide. | 2010-12-11 |
|
| 3-[(E)-2-Chloro-3,3,3-trifluoro-prop-1-en-1-yl]-N-(2-fluoro-phen-yl)-2,2-dimethyl-cyclo-propane-1-carboxamide. | 2010-12-11 |
|
| Synthesis of chitin cycloalkyl ester derivatives and their physical properties. | 2010-09-23 |
|
| The 5' untranslated region of the VR-ACS1 mRNA acts as a strong translational enhancer in plants. | 2010-08 |
|
| Chiral alpha-aminoxy acid/achiral cyclopropane alpha-aminoxy acid unit as a building block for constructing the alpha N-O helix. | 2010-07-16 |
|
| Synthesis and SAR of 2-phenyl-1-sulfonylaminocyclopropane carboxylates as ADAMTS-5 (Aggrecanase-2) inhibitors. | 2009-11-01 |
|
| The synthesis and photoactivated cytotoxicity of 2-methyl-4-oxo-3-prop-2-yn-1-ylcyclopent-2-en-1-yl-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate conjugated with alpha-terthienyl derivatives. | 2009-09-04 |
|
| (E)-2-(2-Chloro-3,3,3-trifluoro-prop-1-en-yl)-N-(2,4-dimethyl-phen-yl)-3,3-dimethyl-cyclo-propane-1-carboxamide. | 2009-06-06 |
|
| Identification, characterization and utilization of unigene derived microsatellite markers in tea (Camellia sinensis L.). | 2009-05-11 |
|
| Potential energy scans and vibrational assignments of cyclopropanecarboxylic acid and cyclopropanecarboxamide. | 2008-12-15 |
|
| Tandem cyclopropanation with dibromomethane under Grignard conditions. | 2008-10-03 |
|
| Direct quantitation of fatty acids present in bacteria and fungi: stability of the cyclopropane ring to chlorotrimethylsilane. | 2008-07-09 |
|
| A new sigma ligand, (+/-)-PPCC, antagonizes kappa opioid receptor-mediated antinociceptive effect. | 2008-03-12 |
|
| Practical, general, and systematic method for optical resolution of gem-dihalo- and monohalocyclopropanecarboxylic acids utilizing chiral 1,1'-binaphtholmonomethyl ethers: application to the synthesis of three chiral pesticides. | 2008-02-07 |
|
| Cyclopropanecarboxylic acid esters as potential prodrugs with enhanced hydrolytic stability. | 2008-02-07 |
|
| (E)-3-(2-Chloro-3,3,3-trifluoro-prop-1-en-yl)-2,2-dimethyl-N,N-diphenyl-cyclo-propane-carboxamide. | 2007-12-06 |
|
| Investigating the mechanistic basis for hepatic toxicity induced by an experimental chemokine receptor 5 (CCR5) antagonist using a compendium of gene expression profiles. | 2007-06 |
|
| Enantioseparation and determination of 2,2-dimethylcyclopropanecarboxamide and corresponding acid in the bioconversion broth by gas chromatography. | 2007-06 |
|
| Reaction pathways of the diketonitrile degradate of isoxaflutole with hypochlorite in water. | 2007-03-07 |
|
| Structural basis for the inhibition of Aurora A kinase by a novel class of high affinity disubstituted pyrimidine inhibitors. | 2007-02-01 |
|
| Enantiomeric differences in permethrin degradation pathways in soil and sediment. | 2006-11-29 |
|
| Towards selective antagonists of T-type calcium channels: design, characterization and potential applications of NNC 55-0396. | 2005 |
|
| Synthetic approach to substituted cyclopropanes based on the coupling reaction of lithiated chloroalkyloxazolines with Fischer carbene complexes. | 2004-08-06 |
|
| Delftia tsuruhatensis sp. nov., a terephthalate-assimilating bacterium isolated from activated sludge. | 2003-09 |
|
| Stereocontrolled synthesis of 3-(trans-2-aminocyclopropyl)alanine, a key component of belactosin A. | 2003-06-26 |
|
| Synthesis and insecticidal activity of novel N-oxydihydropyrrole derivatives with a substituted spirocyclohexyl group. | 2003-06 |
|
| Nitrile biotransformation for highly enantioselective synthesis of 3-substituted 2,2-dimethylcyclopropanecarboxylic acids and amides. | 2003-01-24 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:52:52 GMT 2025
by
admin
on
Mon Mar 31 19:52:52 GMT 2025
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| Record UNII |
008803351S
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| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English |
| Classification Tree | Code System | Code | ||
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EPA PESTICIDE CODE |
688008
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1112
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1759-53-1
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217-162-5
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15655
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008803351S
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C015766
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23500
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DTXSID1040665
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