Recommended Products
Quality Level
assay
97%
bp
126-128 °C/6 mmHg (lit.)
mp
30-32 °C (lit.)
SMILES string
ClCc1ccc(cc1)C(Cl)=O
InChI
1S/C8H6Cl2O/c9-5-6-1-3-7(4-2-6)8(10)11/h1-4H,5H2
InChI key
RCOVTJVRTZGSBP-UHFFFAOYSA-N
Related Categories
Application
4-(Chloromethyl)benzoyl chloride was used as an atom transfer radical polymerization (ATRP) initiator in the growth of polyacrylamide (PAAm) brushes from silicon wafers. It was also used as a building block in a microwave-assisted, solid-phase synthesis of imatinib, an anticancer agent.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
wgk_germany
WGK 3
flash_point_f
199.4 °F
flash_point_c
93 °C
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Journal of fluorescence, 30(4), 867-881 (2020-06-05)
In this study, we developed two different very sensitive magnetite fluorescent Fe3O4@SiO2-TPED-BODIPY and Fe3O4@SiO2-TMPTA-BODIPY nano-sensors for the selective detection of Cr(VI) ions. The Cr(VI) metal ions sensing is based on the fluorescent quenching of BODIPY functionalized with Fe3O4@SiO2-TPED and Fe3O4@SiO2-TMPTA
Tetrahedron Letters, 48, 3455-3455 (2007)
Langmuir : the ACS journal of surfaces and colloids, 23(9), 5120-5126 (2007-03-29)
A method is presented to prevent microbial adhesion to solid surfaces exploiting the unique properties of polymer brushes. Polyacrylamide (PAAm) brushes were grown from silicon wafers by atom transfer radical polymerization (ATRP) using a three-step reaction procedure consisting of immobilization
ACS applied materials & interfaces, 10(43), 36628-36640 (2018-10-10)
CD44 receptor targeting and lipid rafts destroying nanoassembly (NA) was developed for breast cancer therapy. Methyl-β-cyclodextrin (MbCD), as a cholesterol depletion moiety, was conjugated to hyaluronic acid-ceramide (HACE) structure via an ester linkage. HACE-MbCD NA with 198 nm hydrodynamic size
Chemistry (Weinheim an der Bergstrasse, Germany), 24(6), 1348-1357 (2017-11-10)
Gadolinium-loaded nanomicelles show promise as future magnetic resonance imaging (MRI) contrast agents (CAs). Their increased size and high gadolinium (Gd) loading gives them an edge in proton relaxivity over smaller molecular Gd-complexes. Their size and stealth properties are fundamental for
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