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methyl (2,3-di-O-benzyl-4-O-chloroacetyl-α-D-glucopyranosyl bromide)uronate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 87907-01-5 Structure
  • Basic information

    1. Product Name: methyl (2,3-di-O-benzyl-4-O-chloroacetyl-α-D-glucopyranosyl bromide)uronate
    2. Synonyms: methyl (2,3-di-O-benzyl-4-O-chloroacetyl-α-D-glucopyranosyl bromide)uronate
    3. CAS NO:87907-01-5
    4. Molecular Formula:
    5. Molecular Weight: 527.796
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 87907-01-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: methyl (2,3-di-O-benzyl-4-O-chloroacetyl-α-D-glucopyranosyl bromide)uronate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (2,3-di-O-benzyl-4-O-chloroacetyl-α-D-glucopyranosyl bromide)uronate(87907-01-5)
    11. EPA Substance Registry System: methyl (2,3-di-O-benzyl-4-O-chloroacetyl-α-D-glucopyranosyl bromide)uronate(87907-01-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 87907-01-5(Hazardous Substances Data)

87907-01-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87907-01-5 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 87907-01:
(7*8)+(6*7)+(5*9)+(4*0)+(3*7)+(2*0)+(1*1)=165
165 % 10 = 5
So 87907-01-5 is a valid CAS Registry Number.

87907-01-5Relevant 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 HEPARIN FRAGMENTS. A CHEMICAL SYNTHESIS OF THE PENTASACCHARIDE O-(2-DEOXY-2-SULFAMIDO-6-O-SULFO-α-D-GLUCOPYRANOSYL)-(1->4)-O-(β-D-GLUCOPYRANOSYLURONIC ACID)-(1->4)-O-(2-DEOXY-2-SULFAMIDO-3,6-DI-O-SULFO-α-D-GLUCOPYRANOSYL)-(1->4)-O-(2-O-SULFO-

Petitou, Maurice,Duchaussoy, Philippe,Lederman, Isidore,Choay, Jean,Sinay, Pierre,et al.

, p. 221 - 236 (2007/10/02)

Known allyl 4,6-O-benzylidene-α-D-glucopyranoside was first converted into methyl (prop-1-enyl 2,3-di-O-benzyl-4-O-chloroacetyl-α-D-glucopyranosid)-uronate.Acid hydrolysis, followed by treatment with (bromomethylene)dimethylammonium bromide, gave methyl (

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