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139257-77-5

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139257-77-5 Usage

Hazard

A reproductive hazard.

Check Digit Verification of cas no

The CAS Registry Mumber 139257-77-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,2,5 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 139257-77:
(8*1)+(7*3)+(6*9)+(5*2)+(4*5)+(3*7)+(2*7)+(1*7)=155
155 % 10 = 5
So 139257-77-5 is a valid CAS Registry Number.
InChI:InChI=1/C20H30O2/c1-15(8-6-9-17(3)19(22)14-21)11-12-18-16(2)10-7-13-20(18,4)5/h6,8-12,19,21-22H,7,13-14H2,1-5H3/b8-6+,15-11+,17-9+,18-12+

139257-77-5Downstream Products

139257-77-5Relevant articles and documents

Studies on the apoptotic activity of natural and synthetic retinoids: Discovery of a new class of synthetic terphenyls that potently support cell growth and inhibit apoptosis in neuronal and HL-60 cells

Simoni, Daniele,Giannini, Giuseppe,Roberti, Marinella,Rondanin, Riccardo,Baruchello, Riccardo,Rossi, Marcello,Grisolia, Giuseppina,Invidiata, Francesco Paolo,Aiello, Stefania,Marino, Silvia,Cavallini, Sabrina,Siniscalchi, Anna,Gebbia, Nicola,Crosta, Lucia,Grimaudo, Stefania,Abbadessa, Vincenzo,Di Cristina, Antonietta,Tolomeo, Manlio

, p. 4293 - 4299 (2007/10/03)

New terphenyl derivatives have been synthesized and tested for their effect on cell survival in serum-free cultures. These compounds protected HL60 cells from death and supported their growth with an activity higher than that of the natural 14-hydroxy-retro-retinol. Terphenyls 26 and 28 also possess antiapoptotic activity on neuronal cells, proving them as possible candidates for the treatment of neurodegenerative and ischemic diseases.

Practical total syntheses of (R)-(+)- and (S)-(-)-14-hydroxy-4,14-retro- retinol

Nagai,Yoshimura,Hibi,Kikuchi,Abe,Asada,Yamauchi,Hida,Higashi,Hishinuma,Yamanaka

, p. 1545 - 1547 (2007/10/02)

Practical and facile total syntheses of the remarkably unstable (R)-(+)- 14-hydroxy-4, 14-retro-retinol [(R)-14HRR] 1 and of its enantiomer 2 have been achieved via an acid-catalyzed dehydration reaction of the respective tetraeneol intermediates 10 and i

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