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(S)-α-methoxy-N-<(S)-1-phenylethyl>-α-(trifluoromethyl)benzeneacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

140632-13-9

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140632-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 140632-13-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,6,3 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 140632-13:
(8*1)+(7*4)+(6*0)+(5*6)+(4*3)+(3*2)+(2*1)+(1*3)=89
89 % 10 = 9
So 140632-13-9 is a valid CAS Registry Number.

140632-13-9Downstream Products

140632-13-9Relevant academic research and scientific papers

Assignment of absolute stereochemistry to an insect pheromone by chiral amplification

Shi, Xiongwei,Leal, Walter S.,Meinwald, Jerrold

, p. 297 - 303 (2007/10/03)

Chiral amplification, a new strategy for determining the absolute configuration of difficultly available natural secondary alcohols or analogous amines, is described. Using this technique, the R configuration can be assigned to both components of the male

Expeditious synthesis of Mosher amides using a solid supported carbodiimide

Adamczyk, Maciej,Fishpaugh, Jeffrey R.

, p. 7171 - 7172 (2007/10/03)

A novel method of Mosher amide synthesis using a solid supported carbodiimide in CDCl3 is described. Estimation of optical purity can be promptly achieved by direct NMR analysis of the reaction solvent.

Chiral Polymethine Dyes, III. Synthesis and Spectroscopic Properties of an Unsymmetrical, Chiral Monomethine Cyanine Dye with Thiazolyl and Quinolinyl End Group

Reichardt, Christian,Budnik, Ulrich

, p. 927 - 930 (2007/10/02)

The synthesis of the unsymmetrical monomethine cyanine dye 6 in its monochiral (6a, b) and isochiral form (6c), first realized by Goetze in 1938, has been significantly improved and its spectroscopic properties have been studied.According to the synthetic

Enantioselective complexation of organic ammonium ions by simple tetracyclic podand ionophores

Wang, Xuebao,Erickson, Shawn D.,Iimori, Takamasa,Clark Still

, p. 4128 - 4137 (2007/10/02)

A series of enantiomerically pure, C2-symmetric tetracyclic podands are synthesized and studied. These host molecules have methyl substitution, which allows only a few low-energy conformations, and they form well-defined complexes with chiral a

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