About This Item
Produtos recomendados
Nível de qualidade
Ensaio
99%
forma
liquid
índice de refração
n20/D 1.535 (lit.)
pb
198-202 °C (lit.)
pf
−18 °C (lit.)
densidade
1.164 g/mL at 25 °C (lit.)
cadeia de caracteres SMILES
COc1ccc(Cl)cc1
InChI
1S/C7H7ClO/c1-9-7-4-2-6(8)3-5-7/h2-5H,1H3
chave InChI
YRGAYAGBVIXNAQ-UHFFFAOYSA-N
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Descrição geral
4-Chloroanisole is an electron-rich chloroarene. It undergoes Ullmann-type homocoupling catalyzed by in situ generated Pd colloids. Reaction of 4-chloroanisole with Cu(II)-smectite in n-hexane, carbon tetrachloride or dichloromethane has been studied. The nucleophilic photosubstitution reactions, photocyanation and photohydrolysis of 4-chloroanisole has been studied by time resolved spectroscopy.
Código de classe de armazenamento
10 - Combustible liquids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
165.2 °F - closed cup
Ponto de fulgor (°C)
74 °C - closed cup
Equipamento de proteção individual
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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The Journal of organic chemistry, 75(11), 3908-3911 (2010-05-14)
An efficient and highly sustainable Ullmann-type homocoupling of bromo- and chloroarenes, including the more challenging electron-rich chloroarenes (e.g., 4-chloroanisole), catalyzed by in situ generated Pd colloids, is carried out in aqueous medium under relatively mild conditions (temperatures ranging from 40
Laser spectroscopic study of the nucleophilic photosubstitution of 4-chloroanisole and 4-fluoroanisole in aqueous solutions.
Journal of Photochemistry, 30(3), 315-338 (1985)
Single electron transfer mechanism of oxidative dechlorination of 4-chloroanisole on copper (II)-smectite.
Environmental Science & Technology, 21(11), 1119-1123 (1987)
Science advances, 4(5), eaaq0266-eaaq0266 (2018-05-26)
Ether bond activation is very interesting because the synthesis of many valuable compounds involves conversion of ethers. Moreover, C-O bond cleavage is also very important for the transformation of biomass, especially lignin, which abundantly contains ether bonds. Developing efficient methods
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