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Home > Boronic Acids > 1679-18-1

1679-18-1

1679-18-1 | (4-Chlorophenyl)boronic acid

CAS No: 1679-18-1 Catalog No: AG00340A MDL No:MFCD00039137

Product Description

Catalog Number:
AG00340A
Chemical Name:
(4-Chlorophenyl)boronic acid
CAS Number:
1679-18-1
Molecular Formula:
C6H6BClO2
Molecular Weight:
156.3746
MDL Number:
MFCD00039137
IUPAC Name:
(4-chlorophenyl)boronic acid
InChI:
InChI=1S/C6H6BClO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4,9-10H
InChI Key:
CAYQIZIAYYNFCS-UHFFFAOYSA-N
SMILES:
OB(c1ccc(cc1)Cl)O
EC Number:
216-845-5
NSC Number:
25408

Properties

Complexity:
102  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
156.015g/mol
Formal Charge:
0
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
156.372g/mol
Monoisotopic Mass:
156.015g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
40.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0

Literature

Title Journal
Boronic acid library for selective, reversible near-infrared fluorescence quenching of surfactant suspended single-walled carbon nanotubes in response to glucose. ACS nano 20120124
Synthesis of functionalized cinnamaldehyde derivatives by an oxidative Heck reaction and their use as starting materials for preparation of Mycobacterium tuberculosis 1-deoxy-D-xylulose-5-phosphate reductoisomerase inhibitors. The Journal of organic chemistry 20111104
Phenylboronic-acid-based carbohydrate binders as antiviral therapeutics: monophenylboronic acids. Antiviral chemistry & chemotherapy 20100811
Aryl boronic acid inhibition of synthetic melanin polymerization. Bioorganic & medicinal chemistry letters 20100801
Dabco as an inexpensive and highly efficient ligand for palladium-catalyzed Suzuki-Miyaura cross-coupling reaction. Organic letters 20040805

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