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4-nitrophenyl 6-deoxy-6-fluoro-2,3-di-O-α-D-mannopyranosyl-α-D-mannopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

129728-67-2

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129728-67-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129728-67-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,7,2 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 129728-67:
(8*1)+(7*2)+(6*9)+(5*7)+(4*2)+(3*8)+(2*6)+(1*7)=162
162 % 10 = 2
So 129728-67-2 is a valid CAS Registry Number.

129728-67-2Upstream product

129728-67-2Downstream Products

129728-67-2Relevant academic research and scientific papers

SYNTHESIS OF SOME MONODEOOXYFLUORINATED METHYL AND 4-NITROPHENYL α-D-MANNOBIOSIDES AND A RELATED 4-NITROPHENYL α-D-MANNOTRIOSIDE

Khan, Shaheer H.,Jain, Rakesh K.,Abbas, Saeed A.,Matta, Khushi L.

, p. 259 - 273 (1990)

Treatment of methyl 3,4,6-tri-O-benzyl-2-O-(2,3,4-tri-O-acetyl-α-D-mannopyranosyl)-α-D-mannopyranoside with N,N-diethylaminosulfur trifluoride (Et2NSF3), followed by O-deacetylation and catalytic hydrogenolysis, afforded methyl 2-O-(6-deoxy-6-fluoro-α-D-mannopyranosyl)-α-D-mannopyranoside (8).Methyl 6-deoxy-6-fluoro-2-O-α-D-mannopyranosyl-α-D-mannopyranoside (11) was similarly obtained from methyl 3-O-benzyl-2-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl-α-D-mannopyranoside. 1,2,3,4-Tetra-O-acetyl-6-deoxy-6-fluoro-β-D- mannopyranose (13), used for the sythesis of the 4-nitrophenyl analogs of 8 and 11, as well as their 3-O-linked isomers, was obtained by treatment of 1,2,3,4-tetra-O-acetyl-β-D-mannopyranose with Et2NSF3.Treatment of 13 with 4-nitrophenol in the presence of tin(IV) chloride, followed by sequential O-deacetylation, isopropylidenation, acetylation, and cleavage of the acetal group, afforded 4-nitrophenyl 4-O-acetyl-6-deoxy-6-fluoro-α-D-mannopyranoside (18).Treatment of 13 with HBr in glacial acetic acid furnished the 6-deoxy-6-fluoro bromide 19.Glycosylation of diol 18 with 20 gave 4-nitrophenyl 4-O-acetyl-6-deoxy-6-fluoro-3-O-(21) and -2-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-α-D-mannopyranoside (23) in the ratio of ca. 2:1, together with a small proportion of a branched trisaccharide. 4-Nitrophenyl 4,6-di-O-acetyl-α-D-mannopyranoside was similarly glycosylated with bromide 19 to give 4-nitrophenyl 4,6-di-O-acetyl-3-O- and -2-O-(2,3,4-tri-O-acetyl-6-deoxy-6-fluoro-α-D-mannopyranosyl)-α-D-mannopyranoside.The various di- and tri-saccharides were O-deacetylated by Zemplen transesterification.

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