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3-O-benzyl-1,2-O-isopropylidene-α-D-ribo-pentofuranose-4-nitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70448-45-2

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70448-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70448-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,4,4 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 70448-45:
(7*7)+(6*0)+(5*4)+(4*4)+(3*8)+(2*4)+(1*5)=122
122 % 10 = 2
So 70448-45-2 is a valid CAS Registry Number.

70448-45-2Relevant academic research and scientific papers

Facile synthesis of oxo-/thioxopyrimidines and tetrazoles C-C linked to sugars as novel non-toxic antioxidant acetylcholinesterase inhibitors

Figueiredo,Ismael,Pinheiro,Silva,Justino,Silva,Goulart,Mira,Araújo,Campoy,Rauter

, p. 47 - 54 (2012/02/05)

Microwave-assisted synthesis of oxo-/thioxopyrimidines and tetrazoles linked to furanoses with d-xylo and d-ribo configuration, and to a d-galacto pyranose is reported and compared to conventional methods. Reaction of dialdofuranoses and dialdopyranoses w

New one-carbon degradative transformation of β-alkyl-β-azido alcohols

Fan, Qiu-Hua,Ni, Nan-Ting,Li, Qin,Zhang, Li-He,Ye, Xin-Shan

, p. 1007 - 1009 (2007/10/03)

A new transformation of 2-azido-1-hydroxy-containing compounds to nitriles with one carbon less than the starting materials by oxidation was reported. The reaction can be performed under mild conditions.

Bioactive pseudo-C-nucleosides containing thiazole, thiazolidinone, and tetrazole rings

Rauter, Amelia P.,Padilha, Maria,Figueiredo, Jose A.,Ismael, Maria I.,Justino, Jorge,Ferreira, Humberto,Ferreira, Maria J.,Rajendran, Candasamy,Wilkins, Richard,Vaz, Pedro D.,Calhorda

, p. 275 - 296 (2007/10/03)

The synthesis of new pseudo-C-nucleosides was accomplished starting from 3-O-benzyl-1,2-O-isopropylidene-α-D-ribo-pentodialdo-1,4-furanose, aiming to build thiazole, triazole, tetrazole, and thiazolidinone derivatives. The stereochemistry of the thiazolid

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