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87907-02-6

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  • O-(Methyl 2,3-di-o-benzyl-4-chloroacetyl-beta-D-glucopyranosyluronate)-(1-4)-3-0-acetyl-1,6-anhydro-2-azide-2-deoxy-beta-D-glucopyranose

    Cas No: 87907-02-6

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  • O-(Methyl 2,3-di-o-benzyl-4-chloroacetyl-beta-D-glucopyranosyluronate)-(1-4)-3-0-acetyl-1,6-anhydro-2-azide-2-deoxy-beta-D-glucopyranose

    Cas No: 87907-02-6

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  • (2S,3S,4S,5R,6R)-Methyl 6-((1R,2S,3R,4R,5R)-3-acetoxy-4-azido-6,8-dioxabicyclo[3,2,1]octan-2-yloxy)-4,5-bis(benzyloxy)-3-(chlorocarbonyloxy)tetrahydro-2H-pyran-2-carboxylate

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  • C30H32ClN3O12 87907-02-6 (2S,3S,4S,5R,6R)-Methyl 6-((1R,2S,3R,4R,5R)-3-acetoxy-4-azido-6,8-dioxabicyclo[3,2,1]octan-2-yloxy)-4,5-bis(benzyloxy)-3-(chlorocarbonyloxy)tetrahydro-2H-pyran-2-carboxylate

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  • O-[methyl2, 3-di-O-benzyl-4-O-chloroacetyl-beta-Dglucopyranosyluronate]-(1-4)-3-O-acetyl-1, 6-anhydro-2-azido-2-deoxy-beta-D-glucopyranose

    Cas No: 87907-02-6

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87907-02-6 Usage

General Description

The chemical (2S,3S,4S,5R,6R)-Methyl 6-((1R,2S,3R,4R,5R)-3-acetoxy-4-azido-6,8-dioxabicyclo[3,2,1]octan-2-yloxy)-4,5-bis(benzyloxy)-3-(chlorocarbonyloxy)tetrahydro-2H-pyran-2-carboxylate is a complex compound consisting of multiple functional groups and isomers. It contains acetoxy, azido, benzyloxy, and chlorocarbonyloxy moieties, as well as a tetrahydro-2H-pyran-2-carboxylate group. (2S,3S,4S,5R,6R)-Methyl 6-((1R,2S,3R,4R,5R)-3-acetoxy-4-azido-6,8-dioxabicyclo[3,2,1]octan-2-yloxy)-4,5-bis(benzyloxy)-3-(chlorocarbonyloxy)tetrahydro-2H-pyran-2-carboxylate has potential applications in pharmaceuticals, organic synthesis, and material science due to its diverse functional groups and complex structure. Research and development in the field of organic chemistry and drug discovery may benefit from further exploration of the properties and potential uses of this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 87907-02-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,9,0 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 87907-02:
(7*8)+(6*7)+(5*9)+(4*0)+(3*7)+(2*0)+(1*2)=166
166 % 10 = 6
So 87907-02-6 is a valid CAS Registry Number.

87907-02-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name β-D-Glucopyranose, 1,6-anhydro-2-azido-4-O-[4-O-(2-chloroacetyl)-6-methyl-2,3-bis-O-(phenylmethyl)-β-D-glucopyranuronosyl]-2-deoxy-, 3-acetate

1.2 Other means of identification

Product number -
Other names 6,8-Dioxabicyclo[3.2.1]octane, β-D-glucopyranose deriv.

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:87907-02-6 SDS

87907-02-6Downstream Products

87907-02-6Relevant articles and documents

Total synthesis of anticoagulant pentasaccharide fondaparinux

Li, Tiehai,Ye, Hui,Cao, Xuefeng,Wang, Jiajia,Liu, Yonghui,Zhou, Lifei,Liu, Qiang,Wang, Wenjun,Shen, Jie,Zhao, Wei,Wang, Peng

, p. 1071 - 1080 (2014/05/20)

The anticoagulant pentasaccharide fondaparinux was synthesized using an improved and optimized synthetic strategy including a convergent [3+2] coupling approach, orthogonal protecting groups and various glycosyl donors. The new methods of glycosylation were also used for controlling the stereochemical configuration and improving the yield of the glycosylation. In addition, HPLC and NMR methods to monitor the process of total synthesis of fondaparinux were employed. This work provides a comprehensive elaboration for the synthesis and analysis of fondaparinux based on related literature, as well as abundant information for the synthesis of heparin-like oligosaccharides. A matter of protection! The anticoagulant pentasaccharide fondaparinux was synthesized using an improved and optimized synthetic strategy. The process of total synthesis was monitored by HPLC and NMR. This work will contribute to continued improvement of the multistep production of fondaparinux and provide abundant information for the synthesis of heparin-like oligosaccharides.

Synthesis of a heparin pentasaccharide fragment with a high affinity for antithrombin III employing cellobiose as a key starting material

Ichikawa,Monden,Kuzuhara

, p. 611 - 614 (2007/10/02)

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Total synthesis of a heparin pentasaccharide fragment having high affinity for antithrombin III

Sinay, Pierre,Jacquinet, Jean-Claud,Petitou, Maurice,Duchaussoy, Philippe,Lederman, Isidore,et al.

, p. C5 - C18 (2007/10/02)

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