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经验公式(希尔记法):
C10H6ClNO
化学文摘社编号:
分子量:
191.61
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
InChI
1S/C10H6ClNO/c11-10(13)9-6-5-7-3-1-2-4-8(7)12-9/h1-6H
SMILES string
ClC(=O)c1ccc2ccccc2n1
InChI key
WFVMVMAUXYOQSW-UHFFFAOYSA-N
assay
97%
mp
96-98 °C (dec.) (lit.)
functional group
acyl chloride
storage temp.
2-8°C
Quality Level
General description
Quinaldoyl chloride is a quinaldine derivative.
Application
Quinaldoyl chloride may be used to synthesize 5-chloro-2-(2-quinolinecarboxy)acetophenone and benzoin quinaldate.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Synthesis of heterocyclic-substituted chromones and related compounds as potential anticancer agents.
D Donnelly et al.
Journal of medicinal chemistry, 8(6), 872-875 (1965-11-01)
Mechanism of the Acid Catalyzed Formation of Aldehydes from Reissert Compounds.
McEwen WE and Hazlett RN.
Journal of the American Chemical Society, 71(6), 1949-1952 (1949)
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