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1-O-Benzyl-2,3-anhydro-4-O,6-O-benzylidene-α-D-mannopyranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35905-31-8

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35905-31-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35905-31-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,9,0 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 35905-31:
(7*3)+(6*5)+(5*9)+(4*0)+(3*5)+(2*3)+(1*1)=118
118 % 10 = 8
So 35905-31-8 is a valid CAS Registry Number.

35905-31-8Downstream Products

35905-31-8Relevant academic research and scientific papers

Prespacer Glycosides in Glycoconjugate Chemistry. Dibromoisobutyl Glycosides for the Synthesis of Neoglycolipids, Neoglycoproteins, Neoglycparticles, and Soluble Glycosides

Magnusson, Goeran,Ahlfors, Stefan,Dahmen, Jan,Jansson, Karl,Nilsson, Ulf,et al.

, p. 3932 - 3946 (2007/10/02)

3-Bromo-2-(bromomethyl)propyl (dibromoisobutyl or DIB) mono- to tetrasaccharide glycosides were prepared in moderate to high yields by treatment of the corresponding 1-O-acetyl saccharides with 3-bromo-2-(bromomethyl)propanol (DIBOL) and boron trifluoride

Evidence for Bicyclic Oxonium Ions in the Nitrous Acid Deamination of Benzyl 2-Amino-4,6-O-benzylidene-2-deoxy-D-glucopyranosides

Chan, Wai-Pan,Gross, Paul H.

, p. 1369 - 1373 (2007/10/02)

The nitrous acid deamination of conformationally rigid benzyl amino-4,6-O-benzylidenedeoxy-D-hexopyranosides was studied: benzyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-altropyranoside (5) and benzyl 3-amino-4,6-O-benzylidene-3-deoxy-α-D-glucopyranoside (4) in aqueous dioxane both gave some benzyl 2,3-anhydro-4,6-O-benzylidene-α-D-allopyranoside (2).Thus, a trans-diaxial arrangement of hydroxyl and amino groups in the ground state does not appear to be an absolute requirement for epoxide formation, although such an arrangement clearly is most conducive to this reaction, as a comparision of yields showed.Benzyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-mannopyranoside (7) under similar conditions gave, by elimination, benzyl 4,6-O-benzylidene-α-D-erythro-hexopyrano-3-uloside (8) and, by benzyloxy migration, 2-O-benzyl-4,6-O-benzylidene-D-glucopyranose (11).Contrary to expectation, the same products, 8 and 11, were isolated from the deamination of benzyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside (10) and its α-D-mannopyranoside analogue (7).A bicyclic oxonium ion is postulated as an intermediate for the deamination of the α-D-gluco isomer.Benzyl 2-amino-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside (13), with nitrous acid, gave benzyl 4,6-O-benzylidene-2-deoxy-β-D-erythro-hexopyrano-3-uloside (14).Here also, a bicyclic oxonium ion appears to be involved.All products isolated in this or earlier work from the deamination of 2-amino-4,6-O-benzylidene-D-glucopyranosides can be explained by mechanisms involving bicyclic oxonium ion intermediates.Such intermediates are apparently not involved in the deamination of the manno or altro analogues.

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