2-Naphthaleneboronic acid

CAS No.：32316-92-0

Other grades of this product :

2-Naphthaleneboronic acid Basic information

description Uses Solubility Application

Product Name:	2-Naphthaleneboronic acid
Synonyms:	AKOS BRN-0020;AKOS BRN-0041;ALPHA-NAPHTHYLBORIC ACID;1-NAPHTHYLENEBORONIC ACID;2-NAPHTHYLBORONIC ACID;2-NAPHTHENEBORONIC ACID;2-NAPHTHALENEYLBORONIC ACID;2-NAPHTHALENEBORONIC ACID
CAS:	32316-92-0
MF:	C10H9BO2
MW:	171.99
EINECS:	628-070-3
Product Categories:	Boronic Acid;Naphthalene;Boron Compounds;Boronic acids;Organoborons;B (Classes of Boron Compounds);Industrial/Fine Chemicals;blocks;BoronicAcids;Boronic Acid series;OLED materials,pharm chemical,electronic;Boronate Ester;Potassium Trifluoroborate
Mol File:	32316-92-0.mol

2-Naphthaleneboronic acid Chemical Properties

Melting point	269-275 °C(lit.)
Boiling point	381.9±25.0 °C(Predicted)
density	1.21±0.1 g/cm3(Predicted)
storage temp.	Keep in dark place,Sealed in dry,Room Temperature
Water Solubility	Slightly soluble in water
pka	8.53±0.30(Predicted)
form	Crystalline Powder and/or Chunks
color	White to off-white
BRN	2936449
InChIKey	KPTRDYONBVUWPD-UHFFFAOYSA-N
CAS DataBase Reference	32316-92-0(CAS DataBase Reference)

Safety Information

Hazard Codes	Xi
Risk Statements	36/37/38
Safety Statements	26-36-37/39
WGK Germany	3
TSCA	No
HazardClass	IRRITANT
HS Code	29319090

MSDS Information

Provider	Language
ACROS	English
SigmaAldrich	English
ALFA	English

2-Naphthaleneboronic acid Usage And Synthesis

description	2-Naphthalene Boronic Acid is an organometallic iridium complex with applications in catalysis and Pharmaceutical manufacturing. It can be also used in the study of an enantioselective rhodium-catalyzed addition of aryl boronic acids to 2,2,2-trifluoroacetophenones leading to chiral, tertiary trifluoromethyl alcohols.
Uses	2-Naphthaleneboronic acid is a useful research chemical for organic synthesis and other chemical processes.
Solubility	Solubility in water: slightly soluble. Other solubilities: soluble in methanol
Application	It is used to study the enantioselective rhodium-catalyzed addition reaction of arylboronic acid and 2,2,2-trifluoroacetophenone to generate chiral tertiary trifluoromethanol. It can also be used to study the palladium-catalyzed addition reaction of arylboronic acid and nitrile to generate aryl ketones, and aromatic adverbial clauses: palladium-catalyzed addition of oxynitrile to benzofuran.
Chemical Properties	yellow crystal powde
Uses	suzuki reaction
Uses	Used in a study of an enantioselective rhodium-catalyzed addition of aryl boronic acids to 2,2,2-trifluoroacetophenones leading to chiral, tertiary trifluoromethyl alcohols. Also employed in a study of a palladium-catalyzed addition of aryl boronic acids to nitriles providing aryl ketones and to aryloxy nitriles providing benzofurans.

2-Naphthaleneboronic acid Preparation Products And Raw materials

Raw materials	Tetrahydrofuran-->n-Butyllithium-->Trimethyl borate-->2-Naphthol-->2-Bromonaphthalene
Preparation Products	10-(2-Naphthyl)anthracene-9-boronic acid-->4-(NAPHTHALEN-2-YL)PHENYLBORONIC ACID -->2-Naphthalenemethanol-->9-Bromo-10-(2-naphthyl)anthracene-->2,2'-DINAPHTHYL KETONE-->B-ACETAMIDONAPHTHALENE-->Benzenamine, 4-(2-naphthalenyl)-

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