417548
4-Chlorophenylboronic acid
95%
Manufacturer: Sigma Aldrich
CAS Number: 1679-18-1
Synonym(S): (p-Chlorophenyl)boronic acid, 4-Chlorobenzeneboronic acid, NSC 25408, p-Chlorobenzeneboronic acid
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 1 G | 417548-1-G | In Stock | ₹ 1,537.15 |
| 10 G | 417548-10-G | In Stock | ₹ 7,718.23 |
| 25 G | 417548-25-G | In Stock | ₹ 15,717.90 |
417548 - 1 G
In Stock
Quantity
1
Base Price: ₹ 1,537.15
GST (18%): ₹ 276.687
Total Price: ₹ 1,813.837
Quality Level
100
Assay
95%
mp
284-289 °C (lit.)
SMILES string
OB(O)c1ccc(Cl)cc1
InChI
1S/C6H6BClO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4,9-10H
InChI key
CAYQIZIAYYNFCS-UHFFFAOYSA-N
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | Aobchem 4-Chlorophenylboronic acid, AOBCHEM USA 10188-100G. 1679-18-1. MFCD00039137 | -- | ₹ 14,345.85 | |
| | Accela Chembio Inc 4-chlorobenzeneboronic Acid | 25g | 1679-18-1 | MFCD00039137 | 98% | Shelf Life: 1260 Days | Light Sensitive/nitrogen Or Argon/+4 | -- | ₹ 2,139.00 | |
| | Sigma Aldrich Fine Chemicals Biosciences 4-Chlorophenylboronic acid 95% | 1679-18-1 | MFCD00039137 | 10G | -- | ₹ 12,892.18 | |
| | Frontier Specialty Chemicals 5g 4-Chlorophenylboronic acid, 1679-18-1 MFCD00039137 | -- | ₹ 2,481.24 | |
| | 4-Chlorophenylboronic Acid (contains varying amounts of Anhydride), TCI America™ | -- | ₹ 5,330.39 | |
| | (4-Chlorophenyl)boronic acid | -- | ₹ 256.68 - ₹ 77,004.00 | |
| | NSC 25408 | -- | ₹ 1,368.96 - ₹ 20,192.16 | |
| | 1679-18-1 | 4-Chlorophenylboronic acid | -- | ₹ 342.24 - ₹ 7,101.48 |
Related Products
Description
- Application: 4-Chlorophenylboronic acid can be used as a reactant in:Palladium-catalyzed direct arylation.[1]Cyclopalladation.[2] Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation.[3] Copper-mediated ligandless aerobic fluoroalkylation.[4] Pd-catalyzed arylative cyclization.[5] Ruthenium catalyzed direct arylation.[6] Ligand-free copper-catalyzed coupling reactions.[7] Regioselective arylation and alkynylation by Suzuki-Miyaura and Sonogashira cross-coupling reactions.[8] It can also be used to prepare: Substituted diarylmethylidenefluorenes via Suzuki coupling reaction.[9]Baclofen lactam by Suzuki coupling of a pyrrolinyl tosylate, followed by hydrogenation reaction.[10]Palladium(II) thiocarboxamide complexes as Suzuki coupling catalysts.[11] Biaryls by Suzuki reactions of aryl chlorides, bromides, and iodides with arylboronic acids.[12]
- Other Notes: Contains a varying amounts of anhydride
SAFETY INFORMATION
Pictograms
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves