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ChemicalBook Product Catalog Chemical Reagents Organic reagents Boric acid 4-Methoxyphenylboronic acid

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4-Methoxyphenylboronic acid

$ 1.00 /1KG

Min. Order1G
Purity99%
Cas No5720-07-0
Supply Ability100KG
Update time2019-07-06

career henan chemical co

career henan chemical co

7YR

China

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Chemical Properties

Product Name	4-Methoxyphenylboronic acid
CAS No	5720-07-0
EC-No	216-845-5
Min. Order	1G
Purity	99%
Supply Ability	100KG
Release date	2019/07/06

AD68

4-Methoxyphenylboronic acid Basic information

Product Name:	4-Methoxyphenylboronic acid
Synonyms:	(4-methoxyphenyl)-boronicaci;p-methoxy-benzeneboronicaci;p-methoxyphenyl-boronicaci;RARECHEM AH PB 0191;P-METHOXYPHENYLBORONIC ACID;p-methoxybenzeneboronic acid;p-Anisylboronic acid;TIMTEC-BB SBB004055
CAS:	5720-07-0
MF:	C7H9BO3
MW:	151.96
EINECS:	216-845-5
Product Categories:	blocks;BoronicAcids;Boronic Acid series;Substituted Boronic Acids;Boronic acids;Heterocyclic Compounds;Boronic Acid;Alkoxy;Aryl;Organoborons;B (Classes of Boron Compounds);organic or inorganic borate;Aromatics;Intermediates;Miscellaneous Reagents;Aryl Boronic Acids;Boronic Acids and Derivatives;Chemical Synthesis;Monosubstituted Aryl Boronic Acids;Organometallic Reagents;Boron Derivatives;Boronate Ester;Potassium Trifluoroborate;Morpholines/Thiomorpholines ,Isoxazoles ,Indazoles
Mol File:	5720-07-0.mol

4-Methoxyphenylboronic acid Chemical Properties

Melting point	204-206 °C(lit.)
storage temp.	Refrigerator (+4°C)
solubility	Soluble in dimethyl sulfoxide and methanol.
form	Crystalline Powder
color	White to light beige
BRN	2936912
CAS DataBase Reference	5720-07-0(CAS DataBase Reference)

Safety Information

Hazard Codes	Xi
Risk Statements	36/37/38
Safety Statements	26-36-37/39
WGK Germany	3
RTECS	CY8975000
Hazard Note	Irritant
HazardClass	IRRITANT
HS Code	29310095

4-Methoxyphenylboronic acid Usage And Synthesis

Chemical Properties	white to light beige crystalline powder
Uses	Reagent used in the preparation of various biological inhibitors.
Uses	Reagent used for• ;Suzuki-Miyaura cross-coupling reactions1 • ;Pd-catalyzed direct arylation2 • ;Highly effective synthesis using palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water3 • ;Palladium-catalyzed stereoselective Heck-type reaction4 • ;Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence5 • ;Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides6 • ;Ruthenium catalyzed direct arylation7 • ;Rh-catalyzed asymmetric conjugate addition8 R
Uses	4-Methoxylphenylboronic Acid is a phenylboronic acid used to investigate boron function in plants.
Uses	suzuki reaction

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