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(1R,1'R,2S,2'S,5R,5'R)-N,N'-[(2S,3S)-1,4-dihydroxybutane-2,3-diyl]bis(2-isopropyl-5-methylcyclohexanecarboxamide) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1607820-39-2

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1607820-39-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1607820-39-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,7,8,2 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1607820-39:
(9*1)+(8*6)+(7*0)+(6*7)+(5*8)+(4*2)+(3*0)+(2*3)+(1*9)=162
162 % 10 = 2
So 1607820-39-2 is a valid CAS Registry Number.

1607820-39-2Downstream Products

1607820-39-2Relevant academic research and scientific papers

Highly enantioselective alkylation of allyl acetates using tartrate-derived bioxazoline ligands

Jayakumar, Samydurai,Prakash, Muthuraj,Balaraman, Kaluvu,Kesavan, Venkitasamy

, p. 606 - 615 (2014/02/14)

Tartrate-derived bioxazoline ligands, which form a five-membered chelate ring with metals, were evaluated for use in the asymmetric allylic alkylation (AAA) reactions of various symmetrical and unsymmetrical allyl acetates. Excellent enantioselectivities

Highly Enantioselective Alkylation of Allyl Acetates Using Tartrate-Derived Bioxazoline Ligands

Jayakumar, Samydurai,Prakash, Muthuraj,Balaraman, Kaluvu,Kesavan, Venkitasamy

, p. 606 - 615 (2015/10/05)

Tartrate-derived bioxazoline ligands, which form a five-membered chelate ring with metals, were evaluated for use in the asymmetric allylic alkylation (AAA) reactions of various symmetrical and unsymmetrical allyl acetates. Excellent enantioselectivities were achieved by using both symmetrical and unsymmetrical allyl acetates. Palladium(II)-catalyzed asymmetric allylic alkylation reactions of various symmetrical and unsymmetrical allyl acetates were achieved by using bioxazoline ligands, which were derived from tartaric acid, to give products with excellent enantioselectivity.

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