Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H10O2 |
| Molecular Weight | 186.2066 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)CC1=CC=C2C=CC=CC2=C1
InChI
InChIKey=VIBOGIYPPWLDTI-UHFFFAOYSA-N
InChI=1S/C12H10O2/c13-12(14)8-9-5-6-10-3-1-2-4-11(10)7-9/h1-7H,8H2,(H,13,14)
| Molecular Formula | C12H10O2 |
| Molecular Weight | 186.2066 |
| 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 |
|---|---|---|
| Auxin influx inhibitors 1-NOA, 2-NOA, and CHPAA interfere with membrane dynamics in tobacco cells. | 2010-08 |
|
| Activity of increased specific and non-specific esterases and glutathione transferases associated with resistance to permethrin in pediculus humanus capitis (phthiraptera: pediculidae) from Argentina. | 2010-01 |
|
| [Genotypical peculiarities of expression of the beta-specific carboxylic ester hydrolase allozymes in Drosophila melanogaster of wild type]. | 2009-03-04 |
|
| Structure and photochemical properties of (mu-alkoxo)bis(mu-carboxylato)diruthenium complexes with naphthylacetate ligands. | 2006-04-03 |
|
| Site-specific carbon isotope analysis of aromatic carboxylic acids by elemental analysis/pyrolysis/isotope ratio mass spectrometry. | 2006 |
|
| Butyrylcholinesterase, paraoxonase, and albumin esterase, but not carboxylesterase, are present in human plasma. | 2005-11-25 |
|
| The Arabidopsis F-box protein TIR1 is an auxin receptor. | 2005-05-26 |
|
| [Growth-regulating activity of N-benzyl- and O-benzyl-containing compounds belonging to a new group of synthetic analogues of natural auxins]. | 2005-04-30 |
|
| The functional role of threonine-205 in the mechanism-based inactivation of P450 2B1 by two ethynyl substrates: the importance of the F helix in catalysis. | 2004-12 |
|
| Effect of the addition of a nonaqueous polar solvent (glycerol) on enzymatic catalysis in reverse micelles. Hydrolysis of 2-naphthyl acetate by alpha-chymotrypsin. | 2004-07-06 |
|
| Remarkably enhanced excimer formation of naphthylacetate in cation-charged gamma-cyclodextrin. | 2003-05-15 |
|
| Feasibility of atmospheric pressure desorption/ionization on silicon mass spectrometry in analysis of drugs. | 2003 |
|
| Identification and quantification of polar naphthalene derivatives in contaminated groundwater of a former gas plant site by liquid chromatography-electrospray ionization tandem mass spectrometry. | 2002-08-23 |
|
| Esterase isozyme polymorphism, specific and nonspecific esterase, syngenic lines development and natural occurrence of a thermostable esterase in the tropical silkworm Bombyx mori L. | 2001-11-01 |
|
| A procedure for the joint evaluation of substrate partitioning and kinetic parameters for reactions catalyzed by enzymes in reverse micellar solutions. I. Hydrolysis of 2-naphthyl acetate catalyzed by lipase in sodium 1,4-bis(2-ethylhexyl) sulphosuccinate (AOT)/buffer/heptane. | 2001-04-15 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:34:42 GMT 2025
by
admin
on
Mon Mar 31 19:34:42 GMT 2025
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| Record UNII |
202H99Z0CE
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| Record Status |
Validated (UNII)
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