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methyl 2-O-benzyl-4,6-O-benzylidene-3-deoxy-α-D-ribo-hexopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50272-14-5

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50272-14-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50272-14-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,2,7 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 50272-14:
(7*5)+(6*0)+(5*2)+(4*7)+(3*2)+(2*1)+(1*4)=85
85 % 10 = 5
So 50272-14-5 is a valid CAS Registry Number.

50272-14-5Downstream Products

50272-14-5Relevant academic research and scientific papers

Mannose-binding geometry of pradimicin A

Nakagawa, Yu,Doi, Takashi,Taketani, Takara,Takegoshi,Igarashi, Yasuhiro,Ito, Yukishige

, p. 10516 - 10525 (2013/08/23)

Pradimicins (PRMs) and benanomicins are the only family of non-peptidic natural products with lectin-like properties, that is, they recognize D-mannopyranoside (Man) in the presence of Ca2+ ions. Coupled with their unique Man binding ability, t

Total synthesis of actinobolin from d-glucose by way of the stereoselective three-component coupling reaction

Imuta, Satoshi,Tanimoto, Hiroki,Momose, Miho K.,Chida, Noritaka

, p. 6926 - 6944 (2007/10/03)

The total synthesis of (-)-actinobolin 3, an antipode of the natural product, starting from d-glucose is described. A three-component coupling reaction of functionalized cyclohexenone (+)-6 derived from d-glucose by way of Ferrier's carbocyclization react

A Carbohydrate Approach to Polyol Fragments of Amphotericin and the Trienomycin- and Mycotrienin Antibiotics

Fuerstner, Alois,Baumgartner, Judith

, p. 8541 - 8560 (2007/10/02)

Hydrolytically labile ω-chloro-ω-phenylthioglycosides, obtained from the corresponding ω-phenylthioglycosides on treatment with NCS in CCl4, are readily dealkoxyhalogenated with Zn/Ag-graphite in anhydrous solvents affording enantiomerically pure synthons

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