Details
Stereochemistry | ACHIRAL |
Molecular Formula | C7H12O2 |
Molecular Weight | 128.169 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1CCCCC1
InChI
InChIKey=NZNMSOFKMUBTKW-UHFFFAOYSA-N
InChI=1S/C7H12O2/c8-7(9)6-4-2-1-3-5-6/h6H,1-5H2,(H,8,9)
Approval Year
PubMed
Title | Date | PubMed |
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Enhancement and selective production of phoslactomycin B, a protein phosphatase IIa inhibitor, through identification and engineering of the corresponding biosynthetic gene cluster. | 2003 Sep 12 |
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Use of the Rhodopseudomonas palustris genome sequence to identify a single amino acid that contributes to the activity of a coenzyme A ligase with chlorinated substrates. | 2005 Feb |
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The role of syntrophic associations in sustaining anaerobic mineralization of chlorinated organic compounds. | 2005 Mar |
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trans-4-[(2,6-Dimethyl-phen-oxy)methyl]cyclo-hexa-necarboxylic acid. | 2008 Nov 8 |
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Synergistic anti-cancer effects of immunotoxin and cyclosporin in vitro and in vivo. | 2009 Oct 20 |
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Thermostable lipases from the extreme thermophilic anaerobic bacteria Thermoanaerobacter thermohydrosulfuricus SOL1 and Caldanaerobacter subterraneus subsp. tengcongensis. | 2009 Sep |
Patents
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Classification Tree | Code System | Code | ||
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JECFA EVALUATION |
CYCLOHEXANECARBOXYLIC ACID
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H9VKD9VL18
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DTXSID8059180
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m3987
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300000044627
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452
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C044895
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1154649
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CYCLOHEXANECARBOXYLIC ACID
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SUBSTANCE RECORD