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allyl 2,3,4-tri-O-benzoyl-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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  • 374078-99-6 Structure
  • Basic information

    1. Product Name: allyl 2,3,4-tri-O-benzoyl-α-D-mannopyranoside
    2. Synonyms: allyl 2,3,4-tri-O-benzoyl-α-D-mannopyranoside
    3. CAS NO:374078-99-6
    4. Molecular Formula:
    5. Molecular Weight: 532.547
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 374078-99-6.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: allyl 2,3,4-tri-O-benzoyl-α-D-mannopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: allyl 2,3,4-tri-O-benzoyl-α-D-mannopyranoside(374078-99-6)
    11. EPA Substance Registry System: allyl 2,3,4-tri-O-benzoyl-α-D-mannopyranoside(374078-99-6)
  • 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: 374078-99-6(Hazardous Substances Data)

374078-99-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 374078-99-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,4,0,7 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 374078-99:
(8*3)+(7*7)+(6*4)+(5*0)+(4*7)+(3*8)+(2*9)+(1*9)=176
176 % 10 = 6
So 374078-99-6 is a valid CAS Registry Number.

374078-99-6Relevant articles and documents

The composite body deproteinizing chitosanoligosaccharide-

-

, (2016/10/09)

Provided herein are conjugates comprising a protein and an oligosaccharide of one of Formulae I-VI. Also provided herein are pharmaceutical compositions comprising such conjugates. Further provided herein are methods of treating a lysosomal storage disorder in a mammal by administration of an oligosaccharide-glycoprotein conjugate.

Novel template-assembled oligosaccharide clusters as epitope mimics for HIV-neutralizing antibody 2G12. Design, synthesis, and antibody binding study

Wang, Jingsong,Li, Hengguang,Zou, Guozhang,Wang, Lai-Xi

, p. 1529 - 1540 (2008/02/05)

The synthesis of a new class of template-assembled oligomannose clusters as the mimics of the epitope of the HIV-neutralizing antibody 2G12 is described. The novel oligomannose clusters were successfully assembled on a cyclic decapeptide template using th

First synthesis of the immunodominant β-galactofuranose-containing tetrasaccharide present in the cell wall of Aspergillus fumigatus

Fu, Mingkun,Zhang, Guohua,Ning, Jun

, p. 25 - 30 (2007/10/03)

β-Galf-(1→5)-β-Galf-(1→6)-α-Manp-(1→6) -α-Manp, the immunodominant epitope in the cell-wall galactomannan of Aspergillus fumigatus, was synthesized for the first time as its allyl glycoside. The key disaccharide glycosyl donor, 2,3,5,6-tetra-O-benzoyl-β-

Synthesis of a mannotetraose - The repeating unit of the cell-wall mannans of Microsporum gypseum and related species of Trychophyton

Heng, Linsen,Ning, Jun,Kong, Fanzuo

, p. 285 - 296 (2007/10/03)

A tetrasaccharide, α-D-mannopyranosyl-(1→2)-α-D-mannopyranosyl-(1→6)-α- D-mannopyranosyl-(1→6)-D-mannopyranose (1), the repeating unit of the cell-wall mannans of Microsporum gypseum and related species of Trychophyton, was synthesized using 6-O-acetyl-2,

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