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93292-42-3

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93292-42-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93292-42-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,9 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 93292-42:
(7*9)+(6*3)+(5*2)+(4*9)+(3*2)+(2*4)+(1*2)=143
143 % 10 = 3
So 93292-42-3 is a valid CAS Registry Number.

93292-42-3Relevant articles and documents

First total synthesis of pro-resolving and tissue-regenerative resolvin sulfido-conjugates

Rodriguez, Ana R.,Spur, Bernd W.

, p. 1662 - 1668 (2017/04/04)

The first total synthesis of the pro-resolving and tissue-regenerative resolvin sulfido-conjugates: 7S,8R,17S-RCTR1, 7S,8R,17S-RCTR2 and 7S,8R,17S-RCTR3, derived from docosahexaenoic acid, has been achieved. Two synthetic approaches are described. Chiral

The total synthesis of 5-oxo-12(s)-hydroxy-6(e),8(z),10(e),14(z)- eicosatetraenoic acid and its 8,9-trans-isomer and their identification in human platelets

Khanapure, Subhash P.,Powell, William S.,Rokach, Joshua

, p. 8976 - 8982 (2007/10/03)

The first total synthesis of 5-oxo-12(S)-hydroxy-6(E),8(Z),10(E), 14(Z)- eicosatetraenoic acid (5-oxo-12-HETE) 6 and its 8-trans-isomer 7 is reported. The synthetic 5-oxo-12-HETE 6 and its 8,9-trans-isomer 7 were used to identify their formation in mixtures of platelets and neutrophils by transcellular metabolism.

Cyclopropane-containing eicosanoids of marine origin. Biomimetic synthesis of constanolactones A and B from the alga Constaninea simplex

White,Jensen

, p. 6224 - 6233 (2007/10/02)

Asymmetric syntheses of 7, a substance isolated from incubation of arachidonic acid with an acetone powder of the coral Plexaura homomalla, and of constanolactones A (9) and B (10), metabolites of the red alga Constantinea simplex, are described. The key

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