[A15657] CAS 1679-18-1 | 4-Chlorobenzeneboronic acid, 98+% | Alfa
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Brand: Alfa Aesar
1679-18-1 | C6H6BClO2 | benzeneboronic acid, p-chloro-
Chemical Identifiers
CAS
1679-18-1
Molecular Weight (g/mol)
156.37
MDL Number
MFCD00039137
Synonym
benzeneboronic acid, p-chloro-
SMILES
OB(O)C1=CC=C(Cl)C=C1
InChI Key
CAYQIZIAYYNFCS-UHFFFAOYSA-N
Molecular Formula
C6H6BClO2
IUPAC Name
(4-chlorophenyl)boronic acid
Specifications
Assay (Aqueous acid-base Titration)
≥98.0 to ≤102.0%
Proton NMR
Conforms to structure
Identification (FTIR)
Conforms
Form
Powder
Assay (HPLC)
≥98.0%
설명
Used as a GC reagent for diols. It is a reagent used for palladium-catalyzed direct arylation, cyclopalladation, tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation, copper-mediated ligandless aerobic fluoroalkylation, Pd-catalyzed arylative cyclization, ruthenium catalyzed direct arylation, ligand-free copper-catalyzed coupling reactions and regioselective arylation and alkynylation by Suzuki-Miyaura and Sonogashira cross-coupling reactions. Also in as a reagent in the preparation of catalysts for Suzuki-Miyaura cross-coupling, palladium(II) thiocarboxamide complexes as Suzuki coupling catalysts, Biaryls by Suzuki reactions of aryl chlorides, bromides, and iodides with arylboronic acids.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Used as a GC reagent for diols. It is a reagent used for palladium-catalyzed direct arylation, cyclopalladation, tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation, copper-mediated ligandless aerobic fluoroalkylation, Pd-catalyzed arylative cyclization, ruthenium catalyzed direct arylation, ligand-free copper-catalyzed coupling reactions and regioselective arylation and alkynylation by Suzuki-Miyaura and Sonogashira cross-coupling reactions. Also in as a reagent in the preparation of catalysts for Suzuki-Miyaura cross-coupling, palladium(II) thiocarboxamide complexes as Suzuki coupling catalysts, Biaryls by Suzuki reactions of aryl chlorides, bromides, and iodides with arylboronic acids.
Used as a GC reagent for diols. It is a reagent used for palladium-catalyzed direct arylation, cyclopalladation, tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation, copper-mediated ligandless aerobic fluoroalkylation, Pd-catalyzed arylative cyclization, ruthenium catalyzed direct arylation, ligand-free copper-catalyzed coupling reactions and regioselective arylation and alkynylation by Suzuki-Miyaura and Sonogashira cross-coupling reactions. Also in as a reagent in the preparation of catalysts for Suzuki-Miyaura cross-coupling, palladium(II) thiocarboxamide complexes as Suzuki coupling catalysts, Biaryls by Suzuki reactions of aryl chlorides, bromides, and iodides with arylboronic acids.
Solubility
Slightly soluble in water. Soluble in DMSO.
Notes
Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
Other References:
Beilstein:2936346
GHS Hazard and Precautionary Statements
Hazard Statements:H302-H315-H319-H335
GHS H StatementH315-H319-H335Causes skin irritation.Causes serious eye irritation.May cause respiratory irritation.
Precautionary Statements:P261-P264b-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P362-P501c
Risk & Safety
TSCA:NoRTECS Number:CY8950000
경고:RUO – Research Use Only
CAS1679-18-1FORMULAC6H6BClO2EINECS216-845-5MDLMFCD00039137
| Pakage | 1g, 25g, 5g |
|---|---|
| brand | Alfa Aesar |
