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(S)-dimethyl 2-bromo-2-(((tert-butoxycarbonyl)amino)(phenyl)methyl)malonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1235511-97-3

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1235511-97-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1235511-97-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,5,5,1 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1235511-97:
(9*1)+(8*2)+(7*3)+(6*5)+(5*5)+(4*1)+(3*1)+(2*9)+(1*7)=133
133 % 10 = 3
So 1235511-97-3 is a valid CAS Registry Number.

1235511-97-3Downstream Products

1235511-97-3Relevant academic research and scientific papers

Magnesium(II)-binaphtholate as a practical chiral catalyst for the enantioselective direct mannich-type reaction with malonates

Hatano, Manabu,Horibe, Takahiro,Ishihara, Kazuaki

, p. 3502 - 3505 (2010)

(Equation Presented). A highly enantioselective direct Mannich-type reaction of aldimines with dialkyl malonates was developed with the use of a Mg(II)-BINOLate salt, which was designed as a cooperative acid-base catalyst that can activate both aldimines and malonates. Optically active β-aminoesters and α-halo-β-aminoesters could be synthesized in high yields and with high enantioselectivities. This inexpensive and practical Mg(II)-BINOLate salt could be used in gram-scale catalysis.

METHOD FOR PRODUCING beta-AMINOCARBONYL COMPOUND

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Paragraph 0045, (2013/04/10)

An optically active β-aminocarbonyl compound is obtained by a Mannich reaction between an aldimine in which: nitrogen is protected and a malonic acid diester, in the presence of optically active BINOL and dialkyl magnesium (in which two alkyl groups are the same or different) in an amount 1 to 2 molar times the amount of the BINOL.

Highly practical BINOL-derived acid-base combined salt catalysts for the asymmetric direct mannich-type reaction

Hatano, Manabu,Ishihara, Kazuaki

experimental part, p. 3785 - 3801 (2011/02/16)

The catalytic asymmetric direct Mannich-type reaction between aldimines and 1,3-dicarbonyl compounds is one of the most important carbon-carbon bond-forming reactions in organic chemistry. The resulting Mannich adducts can be efficiently transformed into pharmaceutically useful, optically active -amino ketones, -amino esters, -lactams, etc. In the course of our study of chiral acid-base combined salt catalysts for asymmetric reactions, we developed a series of simple, practical, chiral BINOL-derived salt catalysts, such as chiral pyridinium 1,1-binaphthyl-2,2-disulfonates 1, chiral lithium(I) binaphtholate 2, chiral magnesium(II) binaphtholate (3), chiral calcium(II) phosphate 4, and chiral phosphoric acid 5, which were particularly effective for direct Mannich-type reactions. 1 Introduction 2 1,1-Binaphthyl-2,2-disulfonic Acid (BINSA)-Pyridinium Salts 3 Lithium(I) Binaphtholate Salts 4 Magnesium(II) Binaphtholate Salts 5 Calcium(II) Phosphate Salts and Chiral Phosphoric Acids 6 Conclusions. Georg Thieme Verlag Stuttgart · New York.

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