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(2S,4S)-4-azido-1-benzyloxycarbonyl-2-tert-butylaminocarbonylpyrrolidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

176047-29-3

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176047-29-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 176047-29-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,0,4 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 176047-29:
(8*1)+(7*7)+(6*6)+(5*0)+(4*4)+(3*7)+(2*2)+(1*9)=143
143 % 10 = 3
So 176047-29-3 is a valid CAS Registry Number.

176047-29-3Relevant academic research and scientific papers

Asymmetric aldol reaction using immobilized proline on mesoporous support

Calderon, Felix,Fernandez, Raquel,Sanchez, Felix,Fernandez-Mayoralas, Alfonso

, p. 1395 - 1403 (2007/10/03)

The aldol reaction of hydroxyacetone with different aldehydes using immobilized proline on a mesoporous support, assisted by heat and microwaves, has been explored. It was found that heterogenized L-proline on MCM-41 catalyzed aldol reactions in both hydr

Heterogenised catalysts on zeolites. Synthesis of new chiral Rh(I) complexes with (2S,4R)-trans-4-RCOO-2-(t-butylaminocarbonyl) pyrrolidines and (2S,4S)-cis-4-RCONH-2-(t-butylaminocarbonyl) pyrrolidines. Heterogenisation on silica and a USY-zeolite and study of the role of support on their catalytic profile in hydrogenation of olefins

Corma,Iglesias,Mohino,Sanchez

, p. 147 - 156 (2007/10/03)

Novel chiral ligands (2S,4R)-2-(t-butylaminocarbonyl)-4-[3-(alkylaminocarbonyl)propanoyloxy]pyrrolidine and (2S,4S)-cis-4-(alkylaminocarbonylamino)-2-(t-butyl-aminocarbonyl)pyrrolidine (4a,b; 9a,b), (a: alkyl = t-butyl; b: alkyl = 3-triethoxysilylpropyl) and their rhodium complexes were synthesised and characterised. The reactions of [{Rh(cod)Cl}2] and [RhCl(PPh3)3] with the chiral ligands in the presence of a non-coordinating anion (PF-6) gave the cationic complexes [Rh(L2)(ligand)][PF6] (L2 = cod, PPh3). The structures of these complexes were elucidated by elemental analyses, IR spectroscopy and 1H, 13C and 31P NMR measurements. The metal complexes bearing a triethoxysilyl group were covalently bonded to silica and modified USY-zeolite and Rh-heterogenised complexes were obtained. A comparative study (homogeneous versus supported) was made for the catalytic activity in hydrogenation reactions.

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