161144
联苯-4-甲酰氯
97%
别名:
4-联苯基甲酰氯
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关于此项目
线性分子式:
C6H5C6H4COCl
化学文摘社编号:
分子量:
216.66
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
237-804-8
Beilstein/REAXYS Number:
472842
MDL number:
Assay:
97%
产品名称
联苯-4-甲酰氯, 97%
InChI key
JPVUWCPKMYXOKW-UHFFFAOYSA-N
InChI
1S/C13H9ClO/c14-13(15)12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9H
SMILES string
ClC(=O)c1ccc(cc1)-c2ccccc2
assay
97%
mp
110-112 °C (lit.)
functional group
acyl chloride
phenyl
Quality Level
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Application
联苯-4-羰基氯化物用于制备新型硫脲化合物，N-（6-甲基吡啶-2-基-氨基甲硫基）联苯-4-羧酰胺。它也用于制备5-CF3-恶唑类似物，2-{4-[2-（2-联苯-4-基-5-三氟甲基-恶唑-4-基）-乙氧基]-苯氧基}-2-甲基丙酸。
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - 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
Alexander G Godfrey et al.
The Journal of organic chemistry, 68(7), 2623-2632 (2003-03-29)
An improved method for the preparation of a series of oxazole-containing dual PPARalpha/gamma agonists is described. A synthetic sequence utilizing a Dakin-West reaction was devised that allows for the introduction of the oxazole ring either late in the synthetic sequence
Theoretical and experimental studies on N-(6-methylpyridin-2-yl-carbamothioyl) biphenyl-4-carboxamide.
Yesilkaynak T, et al.
European Journal of Chemistry, 1(1), 1-5 (2010)
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