417521
3-Chlorophenylboronic acid
≥95%
Synonym(s):
(m-Chlorophenyl)boronic acid, 3-Chlorobenzeneboronic acid, m-Chlorobenzeneboronic acid
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
ClC6H4B(OH)2
CAS Number:
Molecular Weight:
156.37
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
Product Name
3-Chlorophenylboronic acid, ≥95%
InChI
1S/C6H6BClO2/c8-6-3-1-2-5(4-6)7(9)10/h1-4,9-10H
SMILES string
OB(O)c1cccc(Cl)c1
InChI key
SDEAGACSNFSZCU-UHFFFAOYSA-N
assay
≥95%
form
powder
mp
185-189 °C (lit.)
functional group
chloro
Quality Level
Related Categories
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
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
Related Content
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service