448753
4,4′-Bis(chloromethyl)-1,1′-biphenyl
95%
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About This Item
Productos recomendados
Quality Level
assay
95%
form
solid
mp
126 °C (dec.) (lit.)
functional group
chloro
SMILES string
ClCc1ccc(cc1)-c2ccc(CCl)cc2
InChI
1S/C14H12Cl2/c15-9-11-1-5-13(6-2-11)14-7-3-12(10-16)4-8-14/h1-8H,9-10H2
InChI key
INZDTEICWPZYJM-UHFFFAOYSA-N
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Reaction of 4, 4'-bis (chloromethyl)-1, 1'-biphenyl and phenol in two-phase medium via phase-transfer catalysis.
J. Mol. Catal. A: Chem., 264(1), 119-127 (2007)
Chemistry (Weinheim an der Bergstrasse, Germany), 17(4), 1358-1364 (2011-01-19)
Pyrolytic carbon thin films were deposited on quartz plates through a chemical vapor deposition process, by using a biphenyl precursor, 4,4'-bis(chloromethyl-1,1'-biphenyl). The pyrolytic carbons were microporous and catalytic toward reduction of tri-iodide, and the films thus obtained possessed a metallic
Ultrasonics sonochemistry, 21(1), 395-400 (2013-08-27)
The catalytic esterification of sodium 4-hydroxybenzoate with benzyl bromide by ultrasound-assisted solid-liquid phase-transfer catalysis (U-SLPTC) was investigated using the novel dual-site phase-transfer catalyst 4,4'-bis(tributylammoniomethyl)-1,1'-biphenyl dichloride (BTBAMBC), which was synthesized from the reaction of 4,4'-bis(chloromethyl)-1,1'-biphenyl and tributylamine. Without catalyst and in
ChemSusChem, 12(15), 3627-3634 (2019-05-10)
The utilization of biomass is one of the major challenges for the transition from fossil to renewable resources. Often, the separation of the desired product from the reaction mixture is the most energy-intensive step. Liquid-phase adsorption is a promising separation
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