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1,4-bis-[(1R)-2,3,5,6-tetra-O-benzyl-N-benzyloxycarbonyl-1,4-dideoxy-1,4-imino-D-galactitol-1-yl]-2-butene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

884507-79-3

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884507-79-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 884507-79-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,4,5,0 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 884507-79:
(8*8)+(7*8)+(6*4)+(5*5)+(4*0)+(3*7)+(2*7)+(1*9)=213
213 % 10 = 3
So 884507-79-3 is a valid CAS Registry Number.

884507-79-3Downstream Products

884507-79-3Relevant academic research and scientific papers

Convergent and stereoselective synthesis of iminosugar-containing Galf and UDP-Galf mimicks: Evaluation as inhibitors of UDP-Gal mutase

Liautard, Virginie,Desvergnes, Valerie,Itoh, Kenji,Liu, Hung-Wen,Martin, Olivier R.

, p. 3103 - 3115 (2008/09/19)

(Chemical Equation Presented) The synthesis of a UDP-Galf analog incorporating a 1,4-dideoxy-1,4-imino-D-galactitol skeleton α-linked to UMP by a 3C-tether and of a series of related pyrrolidine galactofuranose mimicks is reported. These compounds were obtained by way of the highly stereoselective reaction of silylated nucleophiles with a N-Cbz glucofuranosylamine which afforded the corresponding open-chain product with a 1,2-syn stereochemistry, as predicted from pionneering studies from Kobayashi. Cyclization of these intermediates afforded α-C-glycosides of imino-galactofuranose carrying various functional groups in the aglycone. Further elaboration of the α-C-allyl substituted derivative by cross-metathesis with a uridin-5′-yl vinylphosphonate provided, after deprotection, the desired original UDP-Galf mimicks. Cleavage of the benzyl ether protecting groups in the iminosugar component using BCl3 proved critical to the success of the synthetic plan. Several of the new 1,4-dideoxy-1,4-imino-D-galactitol derivatives were evaluated as inhibitors of UGM (UDP-galactopyranose mutase) from Escherichia coli; however, none of them exhibited less than mM activities toward this enzyme which catalyzes a crucial step of the biosynthesis of galactofuranose-containing bacterial cell-surface glycans.

Stereoselective synthesis of α-C-substituted 1,4-dideoxy-1,4-imino-D- galactitols. Toward original UDP-Galf mimics via cross-metathesis

Liautard, Virginie,Desvergnes, Valerie,Martin, Olivier R.

, p. 1299 - 1302 (2007/10/03)

Various α-C-substituted 1,4-dideoxy-1,4-imino-D-galactitols were prepared efficiently from 1-O-acetyl-2,3,5,6-tetra-O-benzyl-D-glucofuranose by a four-step sequence involving as the key step the highly syn-selective TMSOTf-catalyzed addition of silylated

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