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ChemicalBook Product Catalog Chemical Reagents Organic reagents Boric acid Methyl 4-boronobenzoate

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Methyl 4-boronobenzoate

$ 1.00 /1KG

Min. Order1G
Purity99%
Cas No99768-12-4
Supply Ability100KG
Update time2019-07-06

career henan chemical co

career henan chemical co

7YR

China

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Chemical Properties

Product Name	Methyl 4-boronobenzoate
CAS No	99768-12-4
EC-No	1806241-263-5
Min. Order	1G
Purity	99%
Supply Ability	100KG
Release date	2019/07/06

AD68

Methyl 4-boronobenzoate Basic information

Product Name:	Methyl 4-boronobenzoate
Synonyms:	RARECHEM AH PB 0115;P-(METHOXYCARBONYL)PHENYLBORONIC ACID;METHYL 4-BORONOBENZOATE;AKOS BRN-0122;4-METHOXYCARBONYLBENZENEBORONIC ACID;4-METHOXYCARBONYLPHENYLBORONIC ACID;4-CARBOMETHOXYPHENYLBORONIC ACID;4-METHOXYCATBONYLPHENYLBORONICACID
CAS:	99768-12-4
MF:	C8H9BO4
MW:	179.97
EINECS:	1806241-263-5
Product Categories:	blocks;BoronicAcids;Carboxes;Boronic Acid series;Acids and Derivatives;Boron, Nitrile, Thio,& TM-Cpds;Boronic acids;Aryl;Boronic acid;Organoborons;B (Classes of Boron Compounds);CHIRAL CHEMICALS;Aryl Boronic Acids;Boronic Acids and Derivatives;Chemical Synthesis;Monosubstituted Aryl Boronic Acids;Organometallic Reagents;Boronate Ester;Potassium Trifluoroborate
Mol File:	99768-12-4.mol

Methyl 4-boronobenzoate Chemical Properties

Melting point	197-200 °C(lit.)
storage temp.	0-6°C
solubility	Soluble in methanol.
CAS DataBase Reference	99768-12-4(CAS DataBase Reference)

Safety Information

Hazard Codes	Xi
Risk Statements	36/37/38
Safety Statements	37/39-26
WGK Germany	3
HazardClass	IRRITANT

Methyl 4-boronobenzoate Usage And Synthesis

Chemical Properties	White to light yellow crystal powde
Uses	Reagent used for• ;Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence1 • ;Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides2 • ;One-pot ipso-nitration of arylboronic acids3 • ;Copper-catalyzed nitration4 • ;Cyclocondensation followed by palladium-phosphine-catalyzed Suzuki-Miyaura coupling5 • ;Reagent used in Preparation of• ;Biaryls via nickel-catalyzed Suzuki-Miyaura cross-coupling reaction of aryl halides with arylboronic acid6† • ;Chromenones and their
Uses	suzuki reaction

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