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2-(2-Fluoro-5-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1192045-84-3

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1192045-84-3 Usage

Type of compound

boronic ester

Structure

a boron atom bonded to two oxygen atoms and a phenyl ring with a fluoro and methyl group attached

Use

as a reagent in organic synthesis, particularly in the Suzuki-Miyaura coupling reaction to form carbon-carbon bonds

Properties

stability and selectivity

Importance

in the development of pharmaceuticals and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 1192045-84-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,2,0,4 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1192045-84:
(9*1)+(8*1)+(7*9)+(6*2)+(5*0)+(4*4)+(3*5)+(2*8)+(1*4)=143
143 % 10 = 3
So 1192045-84-3 is a valid CAS Registry Number.

1192045-84-3Downstream Products

1192045-84-3Relevant academic research and scientific papers

Undirected ortho-selectivity in C–H borylation of arenes catalyzed by NHC platinum(0) complexes

Rzhevskiy, Sergey A.,Topchiy, Maxim A.,Golenko, Yulia D.,Gribanov, Pavel S.,Sterligov, Grigorii K.,Kirilenko, Nikita Yu.,Ageshina, Alexandra A.,Bermeshev, Maxim V.,Nechaev, Mikhail S.,Asachenko, Andrey F.

, p. 569 - 571 (2020/10/09)

Borylation of arenes with bis(pinacolato)diboron catalyzed by sterically encumbered NHC platinum complexes proceeds predominantly at ortho-position even in the absence of a directing group (o: m: p ratio up to 10: 3: 1). The similar borylation with pinacolborane would proceed less selectively.

C(sp2)-H Borylation of Fluorinated Arenes Using an Air-Stable Cobalt Precatalyst: Electronically Enhanced Site Selectivity Enables Synthetic Opportunities

Obligacion, Jennifer V.,Bezdek, Máté J.,Chirik, Paul J.

supporting information, p. 2825 - 2832 (2017/03/08)

Cobalt catalysts with electronically enhanced site selectivity have been developed, as evidenced by the high ortho-to-fluorine selectivity observed in the C(sp2)-H borylation of fluorinated arenes. Both the air-sensitive cobalt(III) dihydride boryl 4-Me-(iPrPNP)Co(H)2BPin (1) and the air-stable cobalt(II) bis(pivalate) 4-Me-(iPrPNP)Co(O2CtBu)2 (2) compounds were effective and exhibited broad functional group tolerance across a wide range of fluoroarenes containing electronically diverse functional groups, regardless of the substitution pattern on the arene. The electronically enhanced ortho-to-fluorine selectivity observed with the cobalt catalysts was maintained in the presence of a benzylic dimethylamine and hydrosilanes, overriding the established directing-group effects observed with precious-metal catalysts. The synthetically useful selectivity observed with cobalt was applied to an efficient synthesis of the anti-inflammatory drug flurbiprofen.

Fluorine-controlled C-H borylation of arenes catalyzed by a PSiN-pincer platinum complex

Takaya, Jun,Ito, Shisei,Nomoto, Hironori,Saito, Narumasa,Kirai, Naohiro,Iwasawa, Nobuharu

supporting information, p. 17662 - 17665 (2015/12/18)

An efficient, regioselective synthesis of fluorine-substituted arylboronic esters was achieved through fluorine-controlled C-H borylation of arenes with diboron catalyzed by a PSiN-platinum complex. The promising utility of the PSiN-platinum catalyst and its unique regioselectivity were demonstrated for the first time, which would complement the well-developed Ir-catalyzed C-H borylation.

Rhodium-catalyzed intermolecular C-H silylation of arenes with high steric regiocontrol

Chen, Cheng,Hartwig, John F.

, p. 853 - 857 (2014/03/21)

Regioselective C-H functionalization of arenes has widespread applications in synthetic chemistry. The regioselectivity of these reactions is often controlled by directing groups or steric hindrance ortho to a potential reaction site. Here, we report a catalytic intermolecular C-H silylation of unactivated arenes that manifests very high regioselectivity through steric effects of substituents meta to a potential site of reactivity. The silyl moiety can be further functionalized under mild conditions but is also inert toward many common organic transformations, rendering the silylarene products useful building blocks. The remote steric effect that we observe results from the steric properties of both the rhodium catalyst and the silane.

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