250260
2-萘甲酰氯
98%
别名:
β-萘甲酰氯
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关于此项目
线性分子式:
C10H7COCl
化学文摘社编号:
分子量:
190.63
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
218-822-5
Beilstein/REAXYS Number:
907776
MDL number:
Assay:
98%
Form:
solid
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
Application
2-萘甲酰氯已被用于：
- 苯丙胺对映体酰胺衍生物的制备
- 7-二甲氨基-2-甲基-3-萘甲氨基-吩噻嗪鎓盐的合成
- （（（（（氨基乙基）氨基）-甲基）苯乙基）三甲氧基硅烷在二氧化硅表面形成的自组装单层的改性
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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)
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
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)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 250260-50G | 04061831829020 |
| 250260-10G | 04061825937359 |