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4-Chlorophenylboronic acid_Molecular_structure_CAS_1679-18-1)
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4-Chlorophenylboronic acid

Catalog No. 417548 Name Sigma Aldrich
CAS Number 1679-18-1 Website http://www.sigmaaldrich.com
M. F. C6H6BClO2 Telephone 1-800-521-8956
M. W. 156.37464 Fax
Purity 95% Email
Storage Chembase ID: 8352

SYNONYMS

Title
4-氯苯基硼酸
IUPAC name
(4-chlorophenyl)boronic acid
IUPAC Traditional name
benzeneboronic acid, p-chloro-
Synonyms
NSC 25408
4-Chlorobenzeneboronic acid
p-Chlorobenzeneboronic acid
(p-Chlorophenyl)boronic acid
4-氯苯硼酸

DATABASE IDS

PubChem SID 24866159
EC Number 216-845-5
MDL Number MFCD00039137
Beilstein Number 2936346
CAS Number 1679-18-1

PROPERTIES

GHS Precautionary statements P280
Risk Statements 20/21/22
RTECS CY8950000
Safety Statements 36
German water hazard class 3
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H302 + H312 + H332
European Hazard Symbols Harmful Harmful (Xn)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
Linear Formula ClC6H4B(OH)2
Purity 95%
Melting Point 284-289 °C(lit.)

DETAILS

Description (English)
Other Notes
Contains a varying amounts of anhydride
Packaging
1, 10 g in glass bottle
25 g in poly bottle
Application
Reagent used for
• Palladium-catalyzed direct arylation1
• Cyclopalladation2
• Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation3
• Copper-mediated ligandless aerobic fluoroalkylation4
• Pd-catalyzed arylative cyclization5
• Ruthenium catalyzed direct arylation6
• Ligand-free copper-catalyzed coupling reactions7
• Regioselective arylation and alkynylation by Suzuki-Miyaura and Sonogashira cross-coupling reactions8 Reagent used in Preparation of
• Catalysts for Suzuki-Miyaura cross-coupling2
• Palladium(II) thiocarboxamide complexes as Suzuki coupling catalysts9
• Biaryls by Suzuki reactions of aryl chlorides, bromides, and iodides with arylboronic acids10
Description (简体中文)
Other Notes
含有不定量的酸酐
包装
1, 10 g in glass bottle
25 g in poly bottle
Application
Reagent used for
• Palladium-catalyzed direct arylation1
• Cyclopalladation2
• Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation3
• Copper-mediated ligandless aerobic fluoroalkylation4
• Pd-catalyzed arylative cyclization5
• Ruthenium catalyzed direct arylation6
• Ligand-free copper-catalyzed coupling reactions7
• Regioselective arylation and alkynylation by Suzuki-Miyaura and Sonogashira cross-coupling reactions8 Reagent used in Preparation of
• Catalysts for Suzuki-Miyaura cross-coupling2
• Palladium(II) thiocarboxamide complexes as Suzuki coupling catalysts9
• Biaryls by Suzuki reactions of aryl chlorides, bromides, and iodides with arylboronic acids10

REFERENCES