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(±)-N-(2-bromoethyl)-N-(cyclohex-2-en-1-yl)-4-methylbenzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

129748-76-1

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129748-76-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129748-76-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,7,4 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 129748-76:
(8*1)+(7*2)+(6*9)+(5*7)+(4*4)+(3*8)+(2*7)+(1*6)=171
171 % 10 = 1
So 129748-76-1 is a valid CAS Registry Number.

129748-76-1Relevant academic research and scientific papers

Formal Bromine Atom Transfer Radical Addition of Nonactivated Bromoalkanes Using Photoredox Gold Catalysis

Zidan, Montserrat,McCallum, Terry,Swann, Rowan,Barriault, Louis

supporting information, p. 8401 - 8406 (2020/11/03)

Organic transformations mediated by photoredox catalysis have been at the forefront of reaction discovery. Recently, it has been demonstrated that binuclear Au(I) bisphosphine complexes, such as [Au2(μ-dppm)2]X2, are capable of mediating electron transfer to nonactivated bromoalkanes for the generation of a variety of alkyl radicals. The transfer reactions of bromine, derived from nonactivated bromoalkanes, are largely unknown. Therefore, we propose that unique metal-based mechanistic pathways are at play, as this binuclear gold catalyst has been known to produce Au(III) Lewis acid intermediates. The scope and proposed mechanistic overview for the formal bromine atom transfer reaction of nonactivated bromoalkanes mediated by photoredox Au(I) catalysis is presented. The methodology presented afforded good yields and a broad scope which include examples using bromoalkanes and iodoarenes.

Synthesis of All-Carbon Quaternary Centers by Palladium-Catalyzed Olefin Dicarbofunctionalization

Koy, Maximilian,Bellotti, Peter,Katzenburg, Felix,Daniliuc, Constantin G.,Glorius, Frank

, p. 2375 - 2379 (2020/01/24)

The redox-neutral dicarbofunctionalization of tri- and tetrasubstituted olefins to form a variety of (hetero)cyclic compounds under photoinduced palladium catalysis is described. This cascade reaction process was used to couple styrenes or acryl amides with a broad range of highly decorated olefins tethered to aryl or alkyl bromides (>50 examples). This procedure enables one or two contiguous all-carbon quaternary centers to be formed in a single step. The products could be readily diversified and applied in the synthesis of a bioactive oxindole analogue.

Palladium-Catalyzed Carbocyclizations of Unactivated Alkyl Bromides with Alkenes Involving Auto-tandem Catalysis

Venning, Alexander R. O.,Kwiatkowski, Megan R.,Roque Pe?a, Joan E.,Lainhart, Brendan C.,Guruparan, Akil A.,Alexanian, Erik J.

, p. 11595 - 11600 (2017/08/30)

The development of a general catalytic system for the palladium-catalyzed carbocyclization of unactivated alkyl bromides with alkenes is described. This approach uses a commercially available bisphosphine ligand and avoids the use of carbon monoxide atmosphere present in prior studies involving alkyl iodides. Detailed mechanistic studies of the transformation are performed, which are consistent with auto-tandem catalysis involving atom-transfer radical cyclization followed by catalytic dehydrohalogenation. These studies also suggest that reactions involving alkyl iodides may proceed through a metal-initiated, rather than metal-catalyzed, radical chain process.

Palladium-catalyzed heck-type reactions of alkyl iodides

Bloome, Kayla S.,McMahen, Rebecca L.,Alexanian, Erik J.

, p. 20146 - 20148 (2012/02/01)

A palladium-catalyzed Heck-type reaction of unactivated alkyl iodides is described. This process displays broad substrate scope with respect to both alkene and alkyl iodide components and provides efficient access to a variety of cyclic products. The reaction is proposed to proceed via a hybrid organometallic-radical mechanism, facilitating the Heck-type process with alkyl halide coupling partners. Initial intermolecular studies are also reported, demonstrating the potentially wide applicability of this approach in synthesis.

VERSATILE METHODS OF SYNTHESIS OF 5 TO 8-MEMBERED RING N-HETEROCYCLES VIA INTRAMOLECULAR CYCLOADDITIONS OF ALLYLAMINES

Rai, K. M. Lokanatha,Hassner, Alfred

, p. 817 - 830 (2007/10/02)

N-Tosylallylamines or homoallylamines were monoalkylated with dibromoalkanes to produce bromoalkylamines 3 or 7.The latter were converted to unsaturated nitro derivatives which, via nitrile oxides, underwent intramolecular cycloaddition to form hetero rin

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