127752
1-Naphthylacetamide
98%
Synonym(s):
1-Naphthaleneacetamide
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About This Item
Linear Formula:
C10H7CH2CONH2
CAS Number:
Molecular Weight:
185.22
Beilstein:
1945547
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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Assay
98%
mp
180-183 °C (lit.)
SMILES string
NC(=O)Cc1cccc2ccccc12
InChI
1S/C12H11NO/c13-12(14)8-10-6-3-5-9-4-1-2-7-11(9)10/h1-7H,8H2,(H2,13,14)
InChI key
XFNJVKMNNVCYEK-UHFFFAOYSA-N
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Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Repr. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Tsung-Rong Kuo et al.
Analytica chimica acta, 699(1), 81-86 (2011-06-28)
A simple technique for quantitative analysis of four urinary biomarkers, tryptophan (TRP), 5-hydroxytryptophan (5-HTP), 5-hydroxytryptamine (5-HT) and 5-hydroxyindole acetic acid (5-HIAA) of carcinoid tumors is developed using gold nanoparticles as the assisted matrix in surface-assisted laser desorption/ionization time-of-flight mass spectrometry
C Ravikumar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 75(2), 859-866 (2010-01-06)
FT Raman and IR spectra of the biologically active molecule, 1-naphthalene acetamide (NA) have been recorded and analyzed. The equilibrium geometry, bonding features and harmonic vibrational wavenumbers of NA have been calculated with the help of B3LYP density functional theory
W P Cochrane et al.
Journal - Association of Official Analytical Chemists, 63(1), 145-148 (1980-01-01)
A simple, rapid, and accurate method has been developed for the determination of naphthalene-acetamide (NAAmide) residues in apples. After extraction with chloroform, separation is performed on an RP-8 high pressure liquid chromatographic column using acetonitrile-water (30 + 70) buffered to
J Shah et al.
Molecular plant-microbe interactions : MPMI, 10(1), 69-78 (1997-01-01)
Salicylic acid (SA) plays an important signaling role in the resistance of many plants to pathogen invasion. Increases in endogenous SA levels have been associated with the hypersensitive response as well as systemic acquired resistance (SAR). SA also induces the
Yoshitaka Arai et al.
Journal of plant research, 117(3), 191-198 (2004-03-26)
The activity of indole-3-acetamide (IAM) hydrolase from rice cells was enriched ca. 628-fold by gel filtration and anion exchange column chromatography. The molecular masses of the IAM hydrolase estimated by gel filtration and sodium dodecyl sulfate polyacrylamide gel electrophoresis were
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