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55124-35-1

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55124-35-1 Usage

Uses

DIPAB, together with DCAB, were developed as cost effective and easy to handle borylation reagents by the Pucheault Group at the Universite de Bordeaux. From aryl and vinyl halide electrophiles, you can easily access the boronic acid derivative of your choice, including BF3K, Bpin and MIDAs.

Check Digit Verification of cas no

The CAS Registry Mumber 55124-35-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,1,2 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55124-35:
(7*5)+(6*5)+(5*1)+(4*2)+(3*4)+(2*3)+(1*5)=101
101 % 10 = 1
So 55124-35-1 is a valid CAS Registry Number.

55124-35-1 Well-known Company Product Price

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  • Aldrich

  • (900347)  Diisopropylamine borane  95%

  • 55124-35-1

  • 900347-1G

  • 497.25CNY

  • Detail
  • Aldrich

  • (900347)  Diisopropylamine borane  95%

  • 55124-35-1

  • 900347-5G

  • 1,490.58CNY

  • Detail

55124-35-1Relevant articles and documents

B-Methylated Amine-Boranes: Substituent Redistribution, Catalytic Dehydrogenation, and Facile Metal-Free Hydrogen Transfer Reactions

Stubbs, Naomi E.,Sch?fer, Andr,Robertson, Alasdair P.M.,Leitao, Erin M.,Jurca, Titel,Sparkes, Hazel A.,Woodall, Christopher H.,Haddow, Mairi F.,Manners, Ian

supporting information, p. 10878 - 10889 (2015/11/27)

Although the dehydrogenation chemistry of amine-boranes substituted at nitrogen has attracted considerable attention, much less is known about the reactivity of their B-substituted analogues. When the B-methylated amine-borane adducts, RR'NH·BH2Me (1a: R = R' = H; 1b: R = Me, R' = H; 1c: R = R' = Me; 1d: R = R' = iPr), were heated to 70 °C in solution (THF or toluene), redistribution reactions were observed involving the apparent scrambling of the methyl and hydrogen substituents on boron to afford a mixture of the species RR'NH·BH3-xMex (x = 0-3). These reactions were postulated to arise via amine-borane dissociation followed by the reversible formation of diborane intermediates and adduct reformation. Dehydrocoupling of 1a-1d with Rh(I), Ir(III), and Ni(0) precatalysts in THF at 20 °C resulted in an array of products, including aminoborane RR'N=BHMe, cyclic diborazane [RR'N-BHMe]2, and borazine [RN-BMe]3 based on analysis by in situ 11B NMR spectroscopy, with peak assignments further supported by density functional theory (DFT) calculations. Significantly, very rapid, metal-free hydrogen transfer between 1a and the monomeric aminoborane, iPr2N=BH2, to yield iPr2NH·BH3 (together with dehydrogenation products derived from 1a) was complete within only 10 min at 20 °C in THF, substantially faster than for the N-substituted analogue MeNH2·BH3. DFT calculations revealed that the hydrogen transfer proceeded via a concerted mechanism through a cyclic six-membered transition state analogous to that previously reported for the reaction of the N-dimethyl species Me2NH·BH3 and iPr2N=BH2. However, as a result of the presence of an electron donating methyl substituent on boron rather than on nitrogen, the process was more thermodynamically favorable and the activation energy barrier was reduced.

Synthesis and the thermal and catalytic dehydrogenation reactions of amine-thioboranes

Robertson, Alasdair P. M.,Haddow, Mairi F.,Manners, Ian

, p. 8254 - 8264 (2012/09/22)

A series of trimethylamine-thioborane adducts, Me3N· BH2SR (R = tBu [2a], nBu [2b], iPr [2c], Ph [2d], C6F 5 [2e]) have been prepared and characterized. Attempts to access secondary and primary amine adducts of thioboranes via amine-exchange reactions involving these species proved unsuccessful, with the thiolate moiety shown to be vulnerable to displacement by free amine. However, treatment of the arylthioboranes, [BH2-SPh]3 (9) and C6F 5SBH2·SMe2 (10) with Me2NH and iPr2NH successfully yielded the adducts Me2NH· BH2SR (R = Ph [11a], C6F5 [12a]) and iPr 2NH·BH2SR (R = Ph [11b], C6F5 [12b]) in high yield. These adducts were also shown to be accessible via thermally induced hydrothiolation of the aminoboranes Me2N=BH 2, derived from the cyclic dimer [Me2N-BH 2]2 (13), and iPr2N=BH2 (14), respectively. Attempts to prepare the aliphatic thiolate substituted adducts R2NH·BH2SR′ (R = Me, iPr; R′ = tBu, nBu, iPr) via this method, however, proved unsuccessful, with the temperatures required to facilitate hydrothiolation also inducing thermal dehydrogenation of the amine-thioborane products to form aminothioboranes, R2N= BH(SR′). Thermal and catalytic dehydrogenation of the targeted amine-thioboranes, 11a/11b and 12a/12b were also investigated. Adducts 11b and 12b were cleanly dehydrogenated to yield iPr2N=BH(SPh) (22) and iPr2N=BH(SC6F5) (23), respectively, at 100 °C (18 h, toluene), with dehydrogenation also possible at 20 °C (42 h, toluene) with a 2 mol % loading of [Rh(μ-Cl)cod]2 in the case of the former species. Similar studies with adduct 11a evidenced a competitive elimination of H2 and HSPh upon thermolysis, and other complex reactivity under catalytic conditions, whereas the fluorinated analogue 12a was found to be resistant to dehydrogenation.

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