Home Other Building Blocks 2-Naphthylacetic acid

2-Naphthylacetic acid

CAS No.:
581-96-4
Catalog Number:
AG003HRP
Molecular Formula:
C12H10O2
Molecular Weight:
186.2066
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$13
- +
5g
98%
In Stock USA
United States
$18
- +
25g
98%
In Stock USA
United States
$43
- +
100g
98%
In Stock USA
United States
$132
- +
Product Description
Catalog Number:
AG003HRP
Chemical Name:
2-Naphthylacetic acid
CAS Number:
581-96-4
Molecular Formula:
C12H10O2
Molecular Weight:
186.2066
MDL Number:
MFCD00004126
IUPAC Name:
2-naphthalen-2-ylacetic acid
InChI:
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)
InChI Key:
VIBOGIYPPWLDTI-UHFFFAOYSA-N
SMILES:
OC(=O)Cc1ccc2c(c1)cccc2
EC Number:
209-475-0
UNII:
202H99Z0CE
NSC Number:
301
Properties
Complexity:
212  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
186.068g/mol
Formal Charge:
0
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
186.21g/mol
Monoisotopic Mass:
186.068g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
37.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.8  
Literature
Title Journal
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Activity of increased specific and non-specific esterases and glutathione transferases associated with resistance to permethrin in pediculus humanus capitis (phthiraptera: pediculidae) from Argentina. Parasitology research 20100101
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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. The Journal of pharmacology and experimental therapeutics 20041201
Effect of the addition of a nonaqueous polar solvent (glycerol) on enzymatic catalysis in reverse micelles. Hydrolysis of 2-naphthyl acetate by alpha-chymotrypsin. Langmuir : the ACS journal of surfaces and colloids 20040706
Remarkably enhanced excimer formation of naphthylacetate in cation-charged gamma-cyclodextrin. Organic letters 20030515
Feasibility of atmospheric pressure desorption/ionization on silicon mass spectrometry in analysis of drugs. Rapid communications in mass spectrometry : RCM 20030101
Identification and quantification of polar naphthalene derivatives in contaminated groundwater of a former gas plant site by liquid chromatography-electrospray ionization tandem mass spectrometry. Journal of chromatography. A 20020823
Esterase isozyme polymorphism, specific and nonspecific esterase, syngenic lines development and natural occurrence of a thermostable esterase in the tropical silkworm Bombyx mori L. Insect biochemistry and molecular biology 20011101
alpha-Ketocarboxylic acid-based inhibitors of protein tyrosine phosphatases. Bioorganic & medicinal chemistry letters 20010723
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. Archives of biochemistry and biophysics 20010415
Properties