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3,4,6-tri-O-benzyl-β-D-mannopyranose 1,2-(pent-4-enyl orthobenzoate) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 125392-62-3 Structure
  • Basic information

    1. Product Name: 3,4,6-tri-O-benzyl-β-D-mannopyranose 1,2-(pent-4-enyl orthobenzoate)
    2. Synonyms: 3,4,6-tri-O-benzyl-β-D-mannopyranose 1,2-(pent-4-enyl orthobenzoate)
    3. CAS NO:125392-62-3
    4. Molecular Formula:
    5. Molecular Weight: 622.758
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 125392-62-3.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: 3,4,6-tri-O-benzyl-β-D-mannopyranose 1,2-(pent-4-enyl orthobenzoate)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,4,6-tri-O-benzyl-β-D-mannopyranose 1,2-(pent-4-enyl orthobenzoate)(125392-62-3)
    11. EPA Substance Registry System: 3,4,6-tri-O-benzyl-β-D-mannopyranose 1,2-(pent-4-enyl orthobenzoate)(125392-62-3)
  • 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: 125392-62-3(Hazardous Substances Data)

125392-62-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125392-62-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,3,9 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 125392-62:
(8*1)+(7*2)+(6*5)+(5*3)+(4*9)+(3*2)+(2*6)+(1*2)=123
123 % 10 = 3
So 125392-62-3 is a valid CAS Registry Number.

125392-62-3Relevant articles and documents

Total synthesis of the fully lipidated glycosylphosphatidylinositol (GPI) anchor of malarial parasite Plasmodium falciparum

Ali, Asif,Vishwakarma, Ram A.

scheme or table, p. 4357 - 4369 (2010/07/06)

We report a new and convergent strategy for the total synthesis of fully lipidated glycosylphosphatidylinositol (GPI) anchor, the major pro-inflammatory factor of malarial parasite (Plasmodium falciparum). The key features of our approach include, the acc

A new approach to construct full-length glycosylphosphatidylinositols of parasitic protozoa and [4-deoxy-Man-III]-GPI analogues

Ali, Asif,Gowda, D. Channe,Vishwakarma, Ram A.

, p. 519 - 521 (2008/09/18)

A new [2 + 2 + 2] approach to construct GPI molecules through the efficient synthesis of glucosamine-inositol and tetramannose intermediates led to a total synthesis of a GPI-anchor of Trypanosoma cruzi, and also afforded a key intermediate for the synthe

One-pot chemo-, regio-, and stereoselective double-differential glycosidation mediated by lanthanide triflates

Jayaprakash,Fraser-Reid, Bert

, p. 4211 - 4214 (2007/10/03)

(Chemical Equation Presented) Nuanced activation of n-pentenyl, thioglycoside, and trichloroacetimidate donors by lanthanide salts coupled with donor/acceptor matching can simplify oligosaccharide assembly. Thus, a one-pot, double-differential glycosidati

Comparing n-pentenyl orthoesters and n-pentenyl glycosides as alternative glycosyl donors

Mach, Mateusz,Schlueter, Urs,Mathew, Felix,Fraser-Reid, Bert,Hazen, Kevin C

, p. 7345 - 7354 (2007/10/03)

As is well known, cyclic 1,2-glycosyl orthoesters undergo ready acid catalyzed rearrangement to 2-O-acyl glycosides in which the alkoxy group is transferred from the orthoester to the anomeric center in a highly stereocontrolled process. The related n-pentenyl derivatives are unique in that either the orthoester (NPOE) or its rearrangement product (NPGAC) can function as a glycosyl donor, and mechanistic considerations indicate that both should (or could!) lead to the same product(s) arising from trans-orthoesterification, glycosidation, glycosyl esterification, etc. Experiments are described which show that the product obtained from a given reaction can be optimized by careful choice of the donor, NPOE or related NPGAC, and careful attention to reaction conditions, electrophilic promoter, 'size' of the glycosyl acceptor, and experimental protocol.

Studies related to synthesis of glycophosphatidylinositol membrane-bound protein anchors. 5. n-pentenyl ortho esters for mannan components

Roberts, Carmichael,Madsen, Robert,Fraser-Reid, Bert

, p. 1546 - 1553 (2007/10/02)

Procedures for rapid assembly of multigram amounts of mannan components have been examined. Although these studies are reported in the context of the mannan moiety of the glycan anchors of membrane-bound glycoproteins, the procedures should be applicable

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