CasNo.5720-07-0,4-methoxyphenylboronic acid 5720-07-0,(5720-07-0) Suppliers

100 Kilogram	Negotiable

Min.Order :100 Kilogram
Purity: 99%
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Keywords

RARECHEM AH PB 0251 5720-07-0 C7H9BO3

Quick Details

Appearance:powder
Application:5720-07-0
PackAge:Depended
ProductionCapacity:300|Kilogram|Month
Storage:Refrigerator
Transportation:by air or by sea

Superiority:

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
Mol File:	5720-07-0.mol

4-Methoxyphenylboronic acid Chemical Properties

mp	204-206 °C(lit.)
storage temp.	Refrigerator (+4°C)
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

MSDS Information

Provider	Language
4-Methoxyphenylboronic acid	English
ACROS	English
SigmaAldrich	English
ALFA	English

4-Methoxyphenylboronic acid Usage And Synthesis

Chemical Properties	white to light beige crystalline powder
Usage	Reagent used in the preparation of various biological inhibitors.
Usage	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
Usage	4-Methoxylphenylboronic Acid is a phenylboronic acid used to investigate boron function in plants.
Usage	suzuki reaction

4-Methoxyphenylboronic acid Preparation Products And Raw materials

Preparation Products

6-(4-METHOXYPHENYL)PYRIDINE-2-CARBALDEHYDE

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