514047
2,3-Dichlorophenylboronic acid
Synonym(s):
(2,3-Dichlorophenyl)dihydroxyborane, 2,3-Dichlorobenzeneboronic acid
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About This Item
Linear Formula:
Cl2C6H3B(OH)2
CAS Number:
Molecular Weight:
190.82
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
InChI
1S/C6H5BCl2O2/c8-5-3-1-2-4(6(5)9)7(10)11/h1-3,10-11H
SMILES string
OB(O)c1cccc(Cl)c1Cl
InChI key
TYIKXPOMOYDGCS-UHFFFAOYSA-N
mp
125 °C (dec.) (lit.)
functional group
chloro
Application
Reactant for:
- Suzuki-Miyaura coupling reactions
- Preparation of biologically and pharmacologically active molecules
Other Notes
Contains varying amounts of anhydride
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Xueshu Li et al.
Environmental science and pollution research international, 25(17), 16402-16410 (2017-05-26)
Nineteen polychlorinated biphenyl (PCB) congeners, such as 2,2',3,3',6-pentachlorobiphenyl (PCB 84), display axial chirality because they form stable rotational isomers, or atropisomers, that are non-superimposable mirror images of each other. Although chiral PCBs undergo atropselective biotransformation and atropselectively alter biological processes
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