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methyl 8,12-anhydro-2,3,4,9,10,11-hexa-O-benzyl-13-O-tert-butyldiphenylsilyl-6,7-dideoxy-α-D-glycero-L-manno-D-galacto-tridec-6(Z)-eno-1,5-pyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

302589-69-1

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302589-69-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 302589-69-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,2,5,8 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 302589-69:
(8*3)+(7*0)+(6*2)+(5*5)+(4*8)+(3*9)+(2*6)+(1*9)=141
141 % 10 = 1
So 302589-69-1 is a valid CAS Registry Number.

302589-69-1Relevant academic research and scientific papers

Improved iterative olefination approach to oligosaccharide mimics: Stereoselective synthesis of β-(1→6)-D-galactopentaose methylene isostere

Dondoni,Mizuno,Marra

, p. 6657 - 6660 (2000)

The title C-pentagalactoside featuring β-(1→6) ethylene bridges between the D-galactopyranose units has been prepared through four consecutive cycles comprising the Wittig reaction of a formyl C-galactoside building block with sugar phosphorane substrate

Linear total synthetic routes to β-D-C-(1,6)-linked oligoglucoses and oligogalactoses up to pentaoses by iterative Wittig olefination assembly

Dondoni, Alessandro,Marra, Alberto,Mizuno, Mamoru,Giovannini, Pier Paolo

, p. 4186 - 4199 (2007/10/03)

Two complementary routes, A and B, have been followed for the stepwise iterative assembly of β-D-(1,6)-glucopyranose and galactopyranose residues through methylene bridges. In route A the building block was constituted by 2,3,4-tri-O-benzyl-6-O-tert-butyldiphenylsilyl (O-TBDPS) β-linked galactosylmethylenephosphorane, while in route B the building block was a β-linked formyl C-glycopyranoside with a similar orthogonal protection of hydroxy groups. In route A each cycle consisted of the reaction of the phosphorane building block with a sugar residue bearing a formyl group at the C-5 carbon atom (coupling) and transformation of the O-TBDPS-protected primary alcohol into the formyl group (arming). Accordingly, route A is defined as the aldehyde route. On the other hand, each cycle in route B involved the coupling of the sugar aldehyde building block with a substrate bearing a phosphorus ylide at C-6 and introduction of the phosphonium group in the arming step as a precursor of the ylide functionality. Accordingly, route B is defined as the ylide route. The efficiency of route A proved to be seriously hampered by the 1,2-elimination of BnOH under the basic reaction conditions of the Wittig olefination, giving rise to the formation of substantial amounts of enopyranose. On the other hand, the ylide route B proved to be more efficient since very good yields (70-93%) of the isolated Wittig products were obtained throughout four consecutive cycles. Individual olefins and polyolefins obtained by routes A and B using gluco and galacto substrates were reduced and debenzylated in one pot by H2/Pd(OH)2 to give the corresponding β-D-C-(1,6)-linked oligosaccharides up to the pentaose stage. The latter compounds were fully characterized by high-field NMR spectroscopy (500 MHz).

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