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N,N,N',N'-tetramethyl ethylene diamine monoborane, also known as TMEDA·BH3, is an organoborane compound that serves as a Lewis acid and a reducing agent. It is formed by the reaction of N,N,N',N'-tetramethylethylenediamine (TMEDA) with boron trifluoride (BF3) or boron trichloride (BCl3), resulting in the formation of a complex with a boron-hydrogen bond. N,N,N',N'-tetramethyl ethylene diamine monoborane is widely used in organic synthesis, particularly in the reduction of carbonyl compounds to form alcohols, and as a catalyst in various chemical reactions. Due to its reactivity, it is typically handled under anhydrous conditions to prevent hydrolysis and is stored in airtight containers to avoid moisture and air exposure.

5843-32-3

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5843-32-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5843-32-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,4 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5843-32:
(6*5)+(5*8)+(4*4)+(3*3)+(2*3)+(1*2)=103
103 % 10 = 3
So 5843-32-3 is a valid CAS Registry Number.

5843-32-3Relevant academic research and scientific papers

Tris(borane) adducts of diphosphanylmethanides: The [H3BCH(PPh2BH3)2]- anion and its alkali metal complexes

Langer, Jens,Geitner, Robert,G?rls, Helmar

, p. 5940 - 5947 (2014)

The reactivity of lithium complexes that contain the borane-modified diphoshanylmethanide ligand [CH(PPh2BH3)2]- towards different Lewis base adducts of BH3 was studied to gain further insight into the mechanism of the isomerization of this derivative, which formally proceeds through a shift of one BH3 group from the phosphorus atom to the carbon atom. Whereas the use of BH3·THF in THF only resulted in the thf adduct of the starting material, [Li{CH(PPh2BH3)2}(thf)2] (1), the application of BH3·SMe2 in toluene resulted in the formation of the novel compound [(Li{H3BCH(PPh2BH3)2})∞] (2). The subsequent addition of ethereal ligands led to the isolation of [Li{H3BCH(PPh2BH3)2}(Me4thf)] (3) and [Li{H3BCH(PPh2BH3)2}(thf)3] (4). Treatment of these complexes with stronger Lewis bases such as N,N,N',N'-tetramethylethane-1,2-diamine (tmeda) results in the removal of one phosphorus-bound BH3 molecule and the formation of the [Ph2PCH(BH3)PPh2BH3]- anion. These results indicate that the isomerization of [CH(PPh2BH3)2]- requires an additional BH3 source and a rather strong Lewis base. Complexes 1-4 and the related derivatives [Li{CH(PPh2BH3)2}(Me4THF)] (5) and [K{H3BCH(PPh2BH3)2}(dme)2] (6; dme = 1,2-dimethoxyethane) were characterized by multinuclear NMR spectroscopy and by single-crystal X-ray diffraction analysis.

Contributions to the Chemistry of Boron, 131. A New Ring System of Boron: 1,4-Dimethyl-1,4-dithionia-2,5-diboratacyclohexane

Noeth, Heinrich,Sedlak, Dieter

, p. 1479 - 1486 (2007/10/02)

(CH3)3N*BH2CH2SCH3 (3) was prepared via Li (2).It reacts with CH3I to yield the sulfonium salt I (4) and decomposes on heating to the title compound 8.The latter contains a six-membered ring in chair conformation and the methyl groups in equatorial positions as revealed by X-ray crystallography.

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