417599

4-Methoxyphenylboronic acid

≥95.0%

Manufacturer: Sigma Aldrich

CAS Number: 5720-07-0

Synonym(S): (4-Methoxyphenyl)boric acid, (p-Methoxyphenyl)boronic acid, 4-Anisylboronic acid, 4-Methoxybenzeneboronic acid, p-Anisylboronic acid, p-Methoxybenzeneboronic acid

Select a Size

Pack Size SKU Availability Price
1 G 417599-1-G In Stock ₹ 2,330.00
5 G 417599-5-G In Stock ₹ 5,740.00
25 G 417599-25-G In Stock ₹ 10,900.78

417599 - 1 G

₹ 2,330.00

In Stock

Quantity

1

Base Price: ₹ 2,330.00

GST (18%): ₹ 419.40

Total Price: ₹ 2,749.40

Quality Level

200

Assay

≥95.0%

form

powder

mp

204-206 °C (lit.)

SMILES string

COc1ccc(cc1)B(O)O

InChI

1S/C7H9BO3/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5,9-10H,1H3

InChI key

VOAAEKKFGLPLLU-UHFFFAOYSA-N

Other Options

Image Product Name Manufacturer Price Range
50-353-216
Accela Chembio Inc 4-methoxyphenylboronic Acid | 100g | 5720-07-0 | MFCD00039139 | 97+% | Shelf Life: 1260 Days | +4
Accela Chembio Inc ₹ 3,217.06
50-179-8808
Sigma Aldrich Fine Chemicals Biosciences 4-Methoxyphenylboronic acid >=95.0% | 5720-07-0 | MFCD00039139 | 5G
Sigma Aldrich Fine Chemicals Biosciences ₹ 8,814.39
50-353-215
Accela Chembio Inc 4-methoxyphenylboronic Acid | 25g | 5720-07-0 | MFCD00039139 | 97+% | Shelf Life: 1260 Days | +4
Accela Chembio Inc ₹ 2,139.00
AR0034SC
4-Methoxybenzeneboronic acid
Aaron Chemicals LLC ₹ 256.68 - ₹ 20,619.96
CS-W002177
4-Methoxyphenylboronic acid
ChemScene ₹ 427.80 - ₹ 12,320.64
AB45072
5720-07-0 | 4-Methoxyphenylboronic acid
A2B Chem ₹ 427.80 - ₹ 8,641.56

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Description

  • Application: Reagent used forSuzuki-Miyaura cross-coupling reactions[1] Pd-catalyzed direct arylation[2] Highly effective synthesis using palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water[3] Palladium-catalyzed stereoselective Heck-type reaction[4] Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence[5] Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides[6] Ruthenium catalyzed direct arylation[7] Rh-catalyzed asymmetric conjugate addition[8] Ligand-free copper-catalyzed coupling[9] Reagent used in Preparation ofPalladium(II) thiocarboxamide complexes as Suzuki coupling catalyst[10] Push-pull arylvinyldiazine chromophores with photophysical properties[11]
  • Other Notes: Contains varying amounts of anhydride

SAFETY INFORMATION

Pictograms

GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Precautionary Statements

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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COc1ccc(cc1)B(O)O

InChI:
1S/C7H9BO3/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5,9-10H,1H3

InChI key:
VOAAEKKFGLPLLU-UHFFFAOYSA-N

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