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(S)-S-ethyl 3-(2'-furyl)-3-[(2'-hydroxyphenyl)amino]propanethioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

192565-63-2

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192565-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 192565-63-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,5,6 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 192565-63:
(8*1)+(7*9)+(6*2)+(5*5)+(4*6)+(3*5)+(2*6)+(1*3)=162
162 % 10 = 2
So 192565-63-2 is a valid CAS Registry Number.

192565-63-2Downstream Products

192565-63-2Relevant academic research and scientific papers

A novel dinuclear chiral niobium complex for Lewis acid catalyzed enantioselective reactions: Design of a tridentate ligand and elucidation of the catalyst structure

Kobayashi, Shu,Arai, Kenzo,Shimizu, Haruka,Ihori, Yoichi,Ishitani, Haruro,Yamashita, Yasuhiro

, p. 761 - 764 (2005)

Two's company: By using a novel chiral ligand a dinuclear chiral niobium catalyst for highly enantioselective Mannich-type reactions was developed. Tridentate binol derivatives provide excellent asymmetric environments around the niobium atom, and the Man

Air-stable, storable, and highly selective chiral Lewis acid catalyst

Ueno, Masaharu,Ishitani, Haruro,Kobayashi, Shu

, p. 3395 - 3397 (2007/10/03)

(matrix presented) An air-stable storable, and highly selective chiral Lewis acid catalyst for asymmetric Mannich-type reactions has been developed. The catalyst can be stored for more than three months in air at room temperature without loss of activity.

Enantioselective mannich-type reactions using a novel chiral zirconium catalyst for the synthesis of optically active β-amino acid derivatives

Ishitani, Haruro,Ueno, Masaharu,Kobayashi, Shu

, p. 8180 - 8186 (2007/10/03)

Catalytic enantioselective Mannich-type reactions of silyl enol ethers with aldimines have been successfully performed using a novel chiral zirconium catalyst prepared from zirconium(IV) tert-butoxide (Zr(OrBu)4), 2 equiv of (R)-6,6'-dibromo-1,

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