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(S)-α-Methyl-N-(6-methyl-2-pyridinylmethylen)phenylmethanamin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53547-65-2

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53547-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53547-65-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,4 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 53547-65:
(7*5)+(6*3)+(5*5)+(4*4)+(3*7)+(2*6)+(1*5)=132
132 % 10 = 2
So 53547-65-2 is a valid CAS Registry Number.

53547-65-2Downstream Products

53547-65-2Relevant academic research and scientific papers

A strategy for the synthesis of well-defined iron catalysts and application to regioselective diene hydrosilylation

Wu, Jessica Y.,Stanzl, Benjamin N.,Ritter, Tobias

supporting information; experimental part, p. 13214 - 13216 (2010/12/19)

We report the development of a well-defined Fe catalyst and its application to the regio-and stereoselective 1,4-hydrosilylation of 1,3-dienes. To the best of our knowledge, this is the first example of accessing a characterized low-valent Fe catalyst by controlled reductive elimination from a readily accessible Fe precatalyst.

Iron-catalyzed 1,4-addition of α-olefins to dienes

Moreau, Benoit,Wu, Jessica Y.,Ritter, Tobias

supporting information; experimental part, p. 337 - 339 (2009/07/04)

Stereo-and Regiosetective 1,4-Addition A new intermolecular, stereo- and regioselective iron-catalyzed 1,4-addition of α-olefins to 1,3-dlenes using as low as 1 mol % of an iminopyridine-ferrous chloride complex was developed. Importantly, both double bon

Synthesis of optically active imidazopyridinium salts and the corresponding NHCs

Schmidt, Michael A.,Movassaghi, Mohammad

, p. 101 - 104 (2007/10/03)

A convergent synthesis of chiral imidazo-[1,5-a]-pyridinium salts is described by facile introduction of a stereogenic center via the N2 substituent. Conversion of these optically active salts to the corresponding N-heterocyclic carbenes (NHCs) and their trapping with sulfur followed by optical activity measurements are discussed.

Asymmetric Catalyses, 14. Enantioselective Hydrosilylation of Prochiral Ketones with Rh- and Pt-Complexes of Optically Active N-Chelate Ligands

Brunner, Henri,Reiter, Barbara,Riepl, Georg

, p. 1330 - 1354 (2007/10/02)

N-chelate ligands with a lateral chiral center, which derive from optically active primary amines, amino acids, and amino acid derivatives, catalyze in Rh and Pt complexes the enantioselective hydrosilylation of acetophenone, benzyl methyl ketone, and tert-butyl methyl ketone with diphenyl- and 1-naphthylphenylsilane.The ketones are transformed into the corresponding silyl ethers which on hydrolysis yield the alcohols 1-phenylethanol, 1-phenyl-2-propanol and 3,3-dimethyl-2-butanol. 37 N ligands 1 - 37 with 2 (I) and K (XX) as well as 21 isolated complexes II - XIX and XXI - XXIII are tested.The best optical inductions exceed considerably those which were obtained with optically active phosphane containing catalysts used up to now.

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