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4-methyl-N-(2-methylene-3-butenyl)benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

210692-83-4

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210692-83-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 210692-83-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,6,9 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 210692-83:
(8*2)+(7*1)+(6*0)+(5*6)+(4*9)+(3*2)+(2*8)+(1*3)=114
114 % 10 = 4
So 210692-83-4 is a valid CAS Registry Number.

210692-83-4Relevant academic research and scientific papers

Missing cyclization pathways and new rearrangements unveiled in the gold(I) and platinum(II)-catalyzed cyclization of 1,6-enynes

Ferrer, Catalina,Raducan, Mihai,Nevado, Cristina,Claverie, Christelle K.,Echavarren, Antonio M.

, p. 6306 - 6316 (2008/02/05)

Cyclopropyl metal carbenes formed in the 6-endo-dig cyclization may evolve to form seven-membered ring intermediates. This has been achieved for the first time by using highly electrophilic platinum(II) and gold(I) complexes. Gold(I) also triggers a remar

Alkynyliodonium salts in organic synthesis. Preparation of annelated dihydropyrroles by cascade addition/bicyclization of dienyltosylamide anions with phenyl(propynyl)iodonium triflate

Feldman, Ken S.,Mareska, David A.

, p. 5650 - 5660 (2007/10/03)

The addition of simple pentadienyltosylamide derivatives to the two- carbon electrophile phenyl(propynyl)iodonium triflate initiates a sequence of transformations that furnishes complex, highly functionalized cyclopentenannelated dihydropyrrole products in moderate yields with complete stereoselection. This sequence demonstrates that diyls resulting from homolytic scission of alkylidene carbene-alkene adducts can be readily accessed under mild experimental conditions and that, in the presence of appropriate pendant functionality, these diyls can productively cyclize. The isomeric isoprene-derived tosylamides follow an abbreviated reaction course and deliver azabicyclo[3.1.0]hexanes via an isomerization that competes with diyl formation.

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