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3-endo-Amino-3-exo-carboxy-menthan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17138-10-2

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17138-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17138-10-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,3 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17138-10:
(7*1)+(6*7)+(5*1)+(4*3)+(3*8)+(2*1)+(1*0)=92
92 % 10 = 2
So 17138-10-2 is a valid CAS Registry Number.

17138-10-2Relevant academic research and scientific papers

Synthesis of a bulky nitroxide and its application in the nitroxide-mediated radical polymerization

Jing, Yuanyuan,Tesch, Matthias,Wang, Lin,Daniliuc, Constantin Gabriel,Studer, Armido

, p. 7665 - 7671 (2016/11/17)

The synthesis of a sterically highly hindered morpholine-based nitroxide is described. Trapping of an α-ester radical with this novel nitroxide leads to an alkoxyamine which is used as an efficient initiator/regulator in the controlled nitroxide-mediated radical polymerization (NMP) of n-butyl acrylate and styrene. Controlled polymerization of n-butyl acrylate can be conducted at very low temperature (50 °C) convincingly documenting the efficiency of this nitroxide for acrylate polymerization.

IBiox[(-)-menthyl]: A sterically demanding chiral NHC ligand

Wuertz, Sebastian,Lohre, Claudia,Froehlich, Roland,Bergander, Klaus,Glorius, Frank

supporting information; experimental part, p. 8344 - 8345 (2009/10/24)

(Figure Presented) An exceedingly sterically demanding, rigid, and chiral NHC ligand, IBiox[(-)-menthyl] (1), was prepared and structurally characterized. With a buried volume of 50percent, this ligand arguably represents one of the most sterically demanding monodentate ligands. The ability to use aryl chloride substrates in intramolecular palladium-catalyzed ,-arylations reveals its unique reactivity. Moreover, C2-symmetric 1 allows the highly enantioselective formation of oxindoles withup to 99percent ee.

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