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139627-54-6

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139627-54-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139627-54-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,6,2 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 139627-54:
(8*1)+(7*3)+(6*9)+(5*6)+(4*2)+(3*7)+(2*5)+(1*4)=156
156 % 10 = 6
So 139627-54-6 is a valid CAS Registry Number.

139627-54-6Relevant articles and documents

Asymmetric Hetero Diels-Alder Reaction Catalyzed by Chiral Ytterbium(III) Phosphate {Yb[(R)-(-)-BNP]3}: Remarkable Ligand Effect on the Enantioselectivity

Hanamoto,Furuno,Sugimoto,Inanaga

, p. 79 - 80 (1997)

2,6-Lutidine was found to be an effective additive for the chiral ytterbium(III) phosphate {Yb[(R)-(-)-BNP]3}-catalyzed asymmetric hetero Diels-Alder reaction thus achieving high enantioselectivity (up to 93% ee) at room temperature.

Highly efficient enantioselective synthesis of optically active dihydropyrones by chiral titanium (iv) (5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2-naphthol) complexes

Wang,Feng,Cui,Liu,Jiang

, p. 1605 - 1606 (2000)

The asymmetric hetero-Diels-Alder reaction of Danishefsky's diene and an aldehyde catalyzed by 20 mol% chiral H8-BINOL-Ti(IV) affords the corresponding 2-substitutent-2,3-dihydro-4H-pyran-4-one with ees of up to 99% under mild reaction conditio

Asymmetric hetero Diels-Alder reaction catalyzed by chromium complexes of heterogeneously hybridized salen/salan ligands

Eno, Satomi,Egami, Hiromichi,Uchida, Tatsuya,Katsuki, Tsutomu

, p. 632 - 633 (2008/12/20)

Various heterogeneously or homogeneously hybridized salen/salan ligands were synthesized, and study of hetero Diels-Alder reactions using their chromium complexes as catalysts revealed that a well-designed heterogeneously hybridized ligand serves as a chi

Methods of performing cycloadditions, reaction mixtures, and methods of performing asymmetric catalytic reactions

-

Page/Page column 23-24; 33-34; 38, (2010/11/27)

Methods of performing cycloadditions are described that include (a) combining a first reactant and a second reactant in a hydrogen bonding solvent to form a reaction mixture; and (b) reacting the first reactant and the second reactant to form a cycloadduc

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