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(2R,3R,4R)-2,3,5-tris(benzyloxy)-4-hydroxypentanal O-(tertbutyldiphenylsilyl)oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

537030-20-9

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537030-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 537030-20-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,7,0,3 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 537030-20:
(8*5)+(7*3)+(6*7)+(5*0)+(4*3)+(3*0)+(2*2)+(1*0)=119
119 % 10 = 9
So 537030-20-9 is a valid CAS Registry Number.

537030-20-9Relevant academic research and scientific papers

Synthesis and glycosidase inhibitory activity of 7-deoxycasuarine

Carmona, Ana T.,Whigtman, Richard H.,Robina, Inmaculada,Vogel, Pierre

, p. 3066 - 3073 (2003)

Reaction of 1,4-anhydro-2,3,5-tri-O-benzyl-1-deoxy-1-imino-D-arabinitol N-oxide (8) with allyl alcohol produced a 3.6:1 mixture of the two pyrrolo[1,2-b]isoxazole derivatives 13 and 14. The major adduct 13 was converted to 7-deoxycasuarine (7), a potent,

Discovery of human hexosaminidase inhibitors by in situ screening of a library of mono- and divalent pyrrolidine iminosugars

Bojarová, Pavla,Carmona, Ana T.,K?en, Vladimír,Kulik, Natalia,Mészáros, Zuzana,Martínez-Bailén, Macarena,Moreno-Vargas, Antonio J.,Pingitore, Valeria,Robina, Inmaculada,Slámová, Kristyna

, (2022/02/14)

Two libraries of mono- and dimeric pyrrolidine iminosugars were synthesized by CuAAC and (thio)urea-bond-forming reactions from the respective azido/aminohexylpyrrolidine iminosugar precursors. The resulting monomeric and dimeric compounds were screened f

Total syntheses of hyacinthacine A2 and 7-deoxycasuarine by cycloaddition to a carbohydrate derived nitrone

Cardona, Francesca,Faggi, Enrico,Liguori, Francesca,Cacciarini, Martina,Goti, Andrea

, p. 2315 - 2318 (2007/10/03)

Practical syntheses of nitrone 8 by two different approaches from sugars are reported. Its use as a versatile intermediate in highly selective 1,3-dipolar cycloaddition reactions constitutes the key step for novel total syntheses of hyacinthacine A2

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