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allyl 2,4,6-tri-O-benzyl-β-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 146773-64-0 Structure
  • Basic information

    1. Product Name: allyl 2,4,6-tri-O-benzyl-β-D-glucopyranoside
    2. Synonyms: allyl 2,4,6-tri-O-benzyl-β-D-glucopyranoside
    3. CAS NO:146773-64-0
    4. Molecular Formula:
    5. Molecular Weight: 490.596
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 146773-64-0.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: allyl 2,4,6-tri-O-benzyl-β-D-glucopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: allyl 2,4,6-tri-O-benzyl-β-D-glucopyranoside(146773-64-0)
    11. EPA Substance Registry System: allyl 2,4,6-tri-O-benzyl-β-D-glucopyranoside(146773-64-0)
  • 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: 146773-64-0(Hazardous Substances Data)

146773-64-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146773-64-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,7,7 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 146773-64:
(8*1)+(7*4)+(6*6)+(5*7)+(4*7)+(3*3)+(2*6)+(1*4)=160
160 % 10 = 0
So 146773-64-0 is a valid CAS Registry Number.

146773-64-0Relevant articles and documents

A Synthetic Route to Epoxyalkyl β-Laminaribiosides, Especially Suitable for Radiolabelling

Best, Wayne M.,Stick, Robert V.,Tilbrook, D. Matthew G.

, p. 1805 - 1810 (2007/10/02)

The major products in the controlled benzylation (NaH/PhCH2Cl) of allyl and but-3-enyl β-D-glucopyranosides were the 2,4,6-tri-O-benzyl ethers.Subsequent glycosidations of these tribenzyl ethers gave derivatives of allyl and but-3-enyl β-laminaribioside,

Dehydrative Glycosylation Using Heptabenzyl Derivatives of Glucobioses and Lactose

Koto, Shinkiti,Morishima, Naohiko,Shichi, Sonoko,Haigoh, Hisamitsu,Hirooka, Motoko,et al.

, p. 3257 - 3274 (2007/10/02)

Dehydrative glycosylations of the 2-, 3-, 4-, and 6-OH groups of D-glucopyranose with hepta-O-benzyl derivatives of glucobioses (O-D-glucopyranosyl-(1->n)-D-glucopyranose; n = 2, 3, 4, or 6) and lactose, in the presence of a ternary mixture of p-nitrobenzenesulfonyl chloride, silver trifluoromethanesulfonate, and triethylamine in dichloromethane showed that the selectivity of the reaction depended on the anomeric configuration and the linking position to the reducing tribenzylglucose moiety of the nonreducing tetrabenzylglucosyl residue and on the class of the OH group to be glycosylated.The use of a quaternary mixture of p-nitrobenzenesulfonyl chloride, silver trifluoromethanesulfonate, N,N-dimethylacetamide, and triethylamine made all but the β(1->2)-linked biosyl donor undergo α-condensation.Several new linear trisaccharides were obtained via debenzylation of the condensates.

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