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p-[2-[N-(p-vinylbenzyl)carbamoyl]ethyl]phenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 359686-23-0 Structure
  • Basic information

    1. Product Name: p-[2-[N-(p-vinylbenzyl)carbamoyl]ethyl]phenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside
    2. Synonyms: p-[2-[N-(p-vinylbenzyl)carbamoyl]ethyl]phenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside
    3. CAS NO:359686-23-0
    4. Molecular Formula:
    5. Molecular Weight: 611.646
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 359686-23-0.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: p-[2-[N-(p-vinylbenzyl)carbamoyl]ethyl]phenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: p-[2-[N-(p-vinylbenzyl)carbamoyl]ethyl]phenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside(359686-23-0)
    11. EPA Substance Registry System: p-[2-[N-(p-vinylbenzyl)carbamoyl]ethyl]phenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside(359686-23-0)
  • 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: 359686-23-0(Hazardous Substances Data)

359686-23-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 359686-23-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,9,6,8 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 359686-23:
(8*3)+(7*5)+(6*9)+(5*6)+(4*8)+(3*6)+(2*2)+(1*3)=200
200 % 10 = 0
So 359686-23-0 is a valid CAS Registry Number.

359686-23-0Relevant articles and documents

Synthesis of new glycopolymers containing β-d-mannopyranose, and c-2-substituted β-d-mannopyranose residues as a new class of inhibitor

Akai, Shoji,Kajihara, Yasuhiro,Nagashima, Yasuhiko,Kamei, Masugu,Arai, Junko,Bito, Masami,Sato, Ken-Ichi

, p. 121 - 143 (2007/10/03)

New styryl monomers containing β-D-mannopyranose, 2-acetamido-2-deoxy-β-D-mannopyranose, 2-deoxy-2-fluoro-β-D-mannopyranose, and 2-deoxy-β-D-arabino-hexopyranose on their side chains, were efficiently synthesized as a new class of a potent inhibitor resistant to exo-α-mannosidase digestion. The binding affinity of the carbohydrate polymers obtained from those mannopyranosyl styryl monomers by radical polymerization with Concanavalin A were evaluated. A binding assay indicated that the multivalency effect and the affinity enhancement attained by modification at the C-2 position of the β-D-mannopyranoside residue resulted in the.

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