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205590-25-6

phenyl 3'-O-benzyl-2,2':4,6:4',6'-tri-O-benzylidene-1-thio-β-laminaribioside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 205590-25-6 Structure

  • Basic information

    1. Product Name: phenyl 3'-O-benzyl-2,2':4,6:4',6'-tri-O-benzylidene-1-thio-β-laminaribioside
    2. Synonyms: phenyl 3'-O-benzyl-2,2':4,6:4',6'-tri-O-benzylidene-1-thio-β-laminaribioside
    3. CAS NO:205590-25-6
    4. Molecular Formula:
    5. Molecular Weight: 788.915
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 205590-25-6.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: phenyl 3'-O-benzyl-2,2':4,6:4',6'-tri-O-benzylidene-1-thio-β-laminaribioside(CAS DataBase Reference)
    10. NIST Chemistry Reference: phenyl 3'-O-benzyl-2,2':4,6:4',6'-tri-O-benzylidene-1-thio-β-laminaribioside(205590-25-6)
    11. EPA Substance Registry System: phenyl 3'-O-benzyl-2,2':4,6:4',6'-tri-O-benzylidene-1-thio-β-laminaribioside(205590-25-6)

  • 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: 205590-25-6(Hazardous Substances Data)

205590-25-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 205590-25-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,5,9 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 205590-25:
(8*2)+(7*0)+(6*5)+(5*5)+(4*9)+(3*0)+(2*2)+(1*5)=116
116 % 10 = 6
So 205590-25-6 is a valid CAS Registry Number.

205590-25-6Relevant articles and documents

Interglycosidic Acetals IV. Preparation and Regioselective Cleavage of Phenyl 2,2′ : 4,6:4′,6′-Tri-O-benzylidene-l-thio-β-laminaribiosides

Sakairi, Nobuo,Okazaki, Yasunori,Furukawa, Jun-Ichi,Kuzuhara, Hiroyoshi,Nishi, Norio,Tokura, Seiichi

, p. 679 - 683 (2007/10/03)

A (+)-10-Camphorsulfonic acid-catalysed acetal exchange reaction of phenyl 1-thio-β-laminaribioside using 3.5 molar equivalents of α,α-dimethoxytoluene gave a tris(benzylidene acetal), which was isolated and characterized as phenyl 3′-O-acetyl-2,2′ 4,6:4′6′-tri-O-benzylidene-1-thio-β-laminaribioside, and the corresponding 3′-O-benzyl derivative 6. Upon a treatment with pyridinium p-toluenesulfonate, the interglycosidic 2,2′-acetal in 6 underwent selective cleavage to give the 2,2′-diol. Additionally, a reductive ring-opening reaction of 6 with lithium aluminium hydride/anhydrous aluminium chloride, followed by O-acetylation, gave the 2,6,6′-O-acetyl-4,2',3',4'-tetra-0-benzyl derivative in 73% yield. A different regioselectivity was observed in the reduction of 6 with borane-trimethylamine adduct/anhydrous aluminium chloride or sodium cyanotrihydroborate/methanesulfonic acid, giving the corresponding 2,4,4′-triol as the major product.

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