Details
Stereochemistry | ACHIRAL |
Molecular Formula | C5H8O2 |
Molecular Weight | 100.1158 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1CCC1
InChI
InChIKey=TXWOGHSRPAYOML-UHFFFAOYSA-N
InChI=1S/C5H8O2/c6-5(7)4-2-1-3-4/h4H,1-3H2,(H,6,7)
Molecular Formula | C5H8O2 |
Molecular Weight | 100.1158 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Cyclobutanecarboxylic acid has been the principal starting material for preparation of monosubstituted cyclobutane derivatives. The urea derivatives of cyclobutanecarboxylic acid have central nervous system depressant qualities while the hydrazines and heterocyclic amides are either inactive or have central nervous system excitatory properties.
Approval Year
PubMed
Title | Date | PubMed |
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Conformation of 2-aminomethylpyrrolidine and 2-aminomethylpiperidine in ternary platinum(II) complexes: regulation of conformation of the diamine by the coexisting ligand. | 2003 Oct |
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Tetra-μ(2)-oxido-di-μ(4)-peroxido-tetra-kis[diphenyl-anti-mony(V)] chloro-form disolvate. | 2009 Feb 6 |
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Total synthesis of punctaporonin C by a regio- and stereoselective [2+2]-photocycloaddition. | 2010 May 25 |
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Synthesis of chitin cycloalkyl ester derivatives and their physical properties. | 2010 Sep 23 |
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/5701682
Cyclobutanecarboxylic acid has low inhibition efficacy on glucose formation from pyruvate by rat kidney slices. At concentration of Cyclobutanecarboxylic acid 0.01 mM glucose formation was inhibited by 9.5%, at 1.0 mM – by 4.4%.
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:42:57 GMT 2023
by
admin
on
Fri Dec 15 19:42:57 GMT 2023
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Record UNII |
0RDJ7C51O0
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Record Status |
Validated (UNII)
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Record Version |
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