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Merck

417521

Sigma-Aldrich

3-Chlorophenylboronic acid

≥95%

Synonym(s):

(m-Chlorophenyl)boronic acid, 3-Chlorobenzeneboronic acid, m-Chlorobenzeneboronic acid

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About This Item

Linear Formula:
ClC6H4B(OH)2
CAS Number:
Molecular Weight:
156.37
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

Assay

≥95%

form

powder

mp

185-189 °C (lit.)

SMILES string

OB(O)c1cccc(Cl)c1

InChI

1S/C6H6BClO2/c8-6-3-1-2-5(4-6)7(9)10/h1-4,9-10H

InChI key

SDEAGACSNFSZCU-UHFFFAOYSA-N

Application

Reactant involved in:
  • 1,4-conjugate addition reactions with ethenesulfonamides to form arylethanesulfonamides
  • Suzuki-Miyaura reactions with dibromotrifluoromethylbenzene
  • Cross-coupling reactions with diazoesters or potassium cyanate
  • Synthesis of biarylketones and phthalides
  • Synthesis of inhibitors including PDE4 inhibitors among others

Other Notes

Contains varying amounts of anhydride

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Junpei Miyake et al.
Science advances, 3(10), eaao0476-eaao0476 (2017-10-28)
Proton exchange membrane fuel cells (PEMFCs) are promising devices for clean power generation in automotive, stationary, and portable applications. Perfluorosulfonic acid (PFSA) ionomers (for example, Nafion) have been the benchmark PEMs; however, several problems, including high gas permeability, low thermal
Chao Zhao et al.
Nucleic acids research, 42(9), e81-e81 (2014-04-01)
The gene- or fragment-specific detection of newly recognized deoxyribonucleic acid (DNA) base 5-hydroxymethylcytosine (5hmC) will provide insights into its critical functions in development and diseases, and is also important for screening 5hmC-rich genes as an indicator of epigenetic states, pathogenic

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