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N-(2,3,4,6-tetra-O-acetyl-α,β-D-galactopyranosyl)aniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

913057-28-0

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913057-28-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 913057-28-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,0,5 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 913057-28:
(8*9)+(7*1)+(6*3)+(5*0)+(4*5)+(3*7)+(2*2)+(1*8)=150
150 % 10 = 0
So 913057-28-0 is a valid CAS Registry Number.

913057-28-0Relevant articles and documents

Synthesis and antiproliferative activity of N-glycosyl-3,3-diaryloxindoles

Kleeblatt, Dennis,Cordes, Christoph A.,Lebrenz, Philipp,Hein, Martin,Feist, Holger,Matin, Abdul,Raza, Rabia,Iqbal, Jamshed,Munshi, Omar,Rahman, Qamar,Villinger, Alexander,Langer, Peter

, p. 22828 - 22839 (2014/06/24)

N-Glycosylated 3,3-diaryloxindoles were prepared by Lewis acid catalyzed reaction of acetylated N-glycosylisatins with various benzene derivatives and subsequent deprotection. Some of the products showed antiproliferative activity against malignant cutane

Synthesis of thia-analogous indirubin n-glycosides and their influence onmelanoma cell growth and apoptosis

Kunz, Manfred,Driller, Katrin M.,Hein, Martin,Libnow, Stephanie,Hohensee, Ina,Ramer, Robert,Hinz, Burkhard,Berger, Anja,Eberle, Juergen,Langer, Peter

scheme or table, p. 534 - 539 (2010/12/25)

Stopping cancer in its tracks Thia-analogues of indirubin-N-glycosides, prepared by condensation of N-glycosylisatines with thiaindane-3-one and subsequent deprotection, were tested for their activity against malignant melanoma cells. These indirubin-N-gl

Synthesis of indirubin-N′-glycosides and their anti-proliferative activity against human cancer cell lines

Libnow, Stefanie,Methling, Karen,Hein, Martin,Michalik, Dirk,Harms, Manuela,Wende, Kristian,Flemming, Anke,Koeckerling, Martin,Reinke, Helmut,Bednarski, Patrick J.,Lalk, Michael,Langer, Peter

, p. 5570 - 5583 (2008/12/20)

The first indirubin-N′-glycosides were prepared based on reactions of isatin-N′-glycosides with indoxyls. The products show a significant anti-proliferative activity against various human cancer cell lines. Good results were observed for an indirubin-N′-mannoside which was shown to have medium to high anti-proliferative activity against all investigated cell lines. The highest activities and selectivities against the MCF-7 breast cancer cell line were observed for indirubin-N′-rhamnosides.

First synthesis of indirubin N-glycosides (red sugars)

Libnow, Stefanie,Hein, Martin,Michalik, Dirk,Langer, Peter

, p. 6907 - 6909 (2007/10/03)

The first indirubin N-glycosides were prepared by reaction of isatine N-glycosides with indoxyl acetate under basic conditions.

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