250260
2-Naphthoyl chloride
98%
Synonym(s):
β-Naphthoyl chloride
Sign Into View Organizational & Contract Pricing
All Photos(3)
About This Item
Linear Formula:
C10H7COCl
CAS Number:
Molecular Weight:
190.63
Beilstein:
907776
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
98%
form
solid
bp
160-162 °C/11 mmHg (lit.)
mp
50-52 °C (lit.)
functional group
acyl chloride
SMILES string
ClC(=O)c1ccc2ccccc2c1
InChI
1S/C11H7ClO/c12-11(13)10-6-5-8-3-1-2-4-9(8)7-10/h1-7H
InChI key
XNLBCXGRQWUJLU-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
Application
2-Naphthoyl chloride has been used in:
- preparation of amide derivatives of the amphetamine enantiomers
- synthesis of 7-dimethylamino-2-methyl-3-naphthamido-phenothiazinium salt
- modification of self-assembled monolayer formed on silica surface from ((((aminoethyl)amino)-methyl)phenethyl)trimethoxysilane
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
235.4 °F - closed cup
Flash Point(C)
113 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
A chemically modified graphite electrode for electrocatalytic oxidation of reduced nicotinamide adenine dinucleotide based on a phenothiazine derivative, 3-?-naphthoyl-toluidine blue O.
Persson B.
J. Electroanal. Chem. Interfac. Electrochem., 287(1), 61-80 (1990)
I W Wainer et al.
Journal of pharmaceutical sciences, 73(8), 1162-1164 (1984-08-01)
A rapid and accurate method was developed for the determination of the enantiomeric composition of amphetamine preparations. Amide derivatives of the amphetamine enantiomers are first formed by using achiral 2-naphthoyl chloride. The resulting enantiomeric amides are then chromatographed on a
V L Lanchote et al.
Journal of chromatography. B, Biomedical applications, 685(2), 281-289 (1996-10-25)
Two methods were developed for the determination of mexiletine enantiomers in plasma samples suitable for studies on the stereoselective disposition of this drug. Both methods used fluorescence detection to improve sensitivity and selectivity. The direct enantioselective separation was based on
Tagbo Emmanuel Ezenwa et al.
Dalton transactions (Cambridge, England : 2003), 47(47), 16938-16943 (2018-11-18)
Selenium and sulfur derivatives of lead(ii) acylchalcogourato complexes have been used to deposit PbSxSe1-x thin films by AACVD. By variation of the mole ratio of sulfur and selenium precursors in the aerosol feed solution the full range of compositions of
Formation and naphthoyl derivatization of aromatic aminosilane self-assembled monolayers: characterization by atomic force microscopy and ultraviolet spectroscopy.
Durfor CN, et al.
Langmuir, 10(1), 148-152 (1994)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service