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4-Methoxycarbonylphenylboronic acid

ALDRICH/594539 - ≥95%

Synonym: (4-Carbomethoxyphenyl)boronic acid; 4-Carbomethoxybenzeneboronic acid; 4-Methoxycarbonylbenzeneboronic acid; 4-borono-benzoic acid 1-methyl ester; p-(Methoxycarbonyl)boronic acid; p-(Methoxycarbonyl)phenylboronic acid; p-borono-benzoic acid methyl ester; Methyl 4-boronobenzoate; Methyl p-boronobenzoate

CAS Number: 99768-12-4
Empirical Formula (Hill Notation): C8H9BO4
Molecular Weight: 179.97
MDL Number: MFCD01632203
Linear Formula: C8H9BO4
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-594539-1G 1 g
 $50.40
1/EA		 Add To Favorites
45-594539-5G 5 g
 $144.00
1/EA		 Add To Favorites
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 594539-1G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 594539-5G

 

assay ≥95%
form powder
functional group ester
InChI 1S/C8H9BO4/c1-13-8(10)6-2-4-7(5-3-6)9(11)12/h2-5,11-12H,1H3
InChI key PQCXFUXRTRESBD-UHFFFAOYSA-N
mp 197-200 °C (lit.)
Quality Level 100 
SMILES string COC(=O)c1ccc(cc1)B(O)O
Application: Reagent used for
• Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence
• Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides
• One-pot ipso-nitration of arylboronic acids
• Copper-catalyzed nitration
• Cyclocondensation followed by palladium-phosphine-catalyzed Suzuki-Miyaura coupling


• Reagent used in Preparation of
• Biaryls via nickel-catalyzed Suzuki-Miyaura cross-coupling reaction of aryl halides with arylboronic acid†
• Chromenones and their bradykinin B1 antagonistic activit†
• Pt nanoparticles@Photoactive metal-organic frameworks resulting in efficient hydrogen evolution via synergistic photoexcitation and electron injectio†
• Salicylate-based thienylbenzoic acids as E. coli methionine aminopeptidase inhibitor†
Other Notes: Contains varying amount of anhydride
Packaging: 1, 5 g in glass bottle
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥95%
mp 197-200 °C (lit.)
UNSPSC 12352103

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