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Borinic acid, bis(4-fluorophenyl)-, 2-aminoethyl ester is a chemical compound with the molecular formula C15H16BF2N. It is an organoborinic acid derivative, featuring a boron atom bonded to two 4-fluorophenyl groups and a 2-aminoethyl ester group. Borinic acid, bis(4-fluorophenyl)-, 2-aminoethyl ester is known for its potential applications in the synthesis of various organic compounds and materials, particularly in the field of pharmaceuticals and agrochemicals. Its unique structure allows for the formation of stable intermediates and catalysts, making it a valuable building block in organic chemistry. The presence of fluorine atoms in the phenyl rings contributes to the compound's reactivity and stability, which can be exploited in various chemical transformations.

2262-43-3

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2262-43-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2262-43-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,6 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2262-43:
(6*2)+(5*2)+(4*6)+(3*2)+(2*4)+(1*3)=63
63 % 10 = 3
So 2262-43-3 is a valid CAS Registry Number.

2262-43-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[bis(4-fluorophenyl)boryloxy]ethylamine

1.2 Other means of identification

Product number -
Other names B,B-Bis(4-fluorphenyl)boroxazolidin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2262-43-3 SDS

2262-43-3Relevant academic research and scientific papers

Borinic acid catalysed peptide synthesis

El Dine, Tharwat Mohy,Rouden, Jacques,Blanchet, Jér?me

supporting information, p. 16084 - 16087 (2015/11/10)

The catalytic synthesis of peptides is a major challenge in the modern organic chemistry hindered by the well-established use of stoichiometric coupling reagents. Herein, we describe for the first time that borinic acid is able to catalyse this reaction under mild conditions with an improved activity compared to our recently developed thiophene-based boronic acid. This catalyst is particularly efficient for peptide bond synthesis affording dipeptides in good yields without detectable racemization.

Cross-coupling of diarylborinic acids and anhydrides with arylhalides catalyzed by a phosphite/N-heterocyclic carbene co-supported palladium catalyst system

Chen, Xiaofeng,Ke, Haihua,Chen, Yao,Guan, Changwei,Zou, Gang

, p. 7572 - 7578 (2012/10/29)

A highly efficient cross-coupling of diarylborinic acids and anhydrides with aryl chlorides and bromides has been effected by using a palladium catalyst system co-supported by a strong σ-donor N-heterocyclic carbene (NHC), N,N′-bis(2,6-diisopropylphenyl) imidazol-2-ylidene, and a strong π-acceptor phosphite, triphenylphosphite, in tert-BuOH in the present of K3PO4·3H2O. Unsymmetrical biaryls with a variety of functional groups could be obtained in good to excellent yields using as low as 0.01, 0.2-0.5, and 1 mol % palladium loadings for aryl bromides and activated and deactivated aryl chlorides, respectively, under mild conditions. A ligand synergy between the σ-donor NHC and the π-acceptor phosphite in the Pd/NHC/P(OPh)3 catalytic system has been proposed to be responsible for the high efficacy to arylchlorides in the cross-coupling. A scalable and economical process has therefore been developed for synthesis of Sartan biphenyl from the Pd/NHC/P(OPh)3 catalyzed cross-coupling of di(4-methylphenyl)borinic acid with 2-chlorobenzonitrile.

DNA Methyltransferase inhibitors

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Page 27, (2008/06/13)

A compound of the formula or a pharmaceutically acceptable salt thereof,whereinR1, R2, and R3 are the same or different and are independently hydrogen, lower alkyl, aryl or substituted aryl, lower alkoxy, lower alkoxyalkyl, or cycloalkyl or cycloalkyl alkoxy, where each cycloalkyl group has from 3-7 members, where up to two of the cycloalkyl members are optionally hetero atoms selected from oxygen and nitrogen, and where any member of the alkyl, aryl or cycloalkyl group is optionally substituted with halogen, lower alkyl or lower alkoxy, aryl or substituted aryl, andwhereR3 can be ribose, deoxyribose or phosphorylated derivatives thereof,whereinR1, R2, and R3 are not all hydrogen andwhereinwhen R3 is ribose, deoxyribose or phosphorylated derivatives thereof, one of R1 or R2 is not hydrogen.

Synthesis and anticoccidial activity of some azacyclo organoborinates

Tabuchi, Hitoshi,Kawaguchi, Harumoto,Taniguchi, Hisashi,Imazaki, Hideyuki,Hayase, Yoshio

, p. 1319 - 1326 (2007/10/03)

A series of azacyclo organoborinates derivatives of piperidinyl and pyridinyl alcohols were prepared and their anticoccidial activity was tested in vitro assay system. Among them, di(4-chlorophenyl)(2-piperidinylmethoxy-O,N)boron, di(3-trifluoromethylphenyl)(2-piperidinylmethoxy-O,N)boron, di(3-trifluoromethylphenyl)(2-pyridinylmethoxy-O,N)boron, and di(3-trifluoromethylphenyl)(2-pyridinylethoxy-O,N)boron, showed moderate anticoccidial activity against Eimeria tenella.

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