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N,N-di-tert-butoxycarbonyl-9-(2’,3’,4’,6’-tetra-O-benzoyl-β-D-glucopyranosyl)adenine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1311109-62-2 Structure
  • Basic information

    1. Product Name: N,N-di-tert-butoxycarbonyl-9-(2’,3’,4’,6’-tetra-O-benzoyl-β-D-glucopyranosyl)adenine
    2. Synonyms: N,N-di-tert-butoxycarbonyl-9-(2’,3’,4’,6’-tetra-O-benzoyl-β-D-glucopyranosyl)adenine
    3. CAS NO:1311109-62-2
    4. Molecular Formula:
    5. Molecular Weight: 913.938
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1311109-62-2.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: N,N-di-tert-butoxycarbonyl-9-(2’,3’,4’,6’-tetra-O-benzoyl-β-D-glucopyranosyl)adenine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N-di-tert-butoxycarbonyl-9-(2’,3’,4’,6’-tetra-O-benzoyl-β-D-glucopyranosyl)adenine(1311109-62-2)
    11. EPA Substance Registry System: N,N-di-tert-butoxycarbonyl-9-(2’,3’,4’,6’-tetra-O-benzoyl-β-D-glucopyranosyl)adenine(1311109-62-2)
  • 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: 1311109-62-2(Hazardous Substances Data)

1311109-62-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1311109-62-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,1,1,0 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1311109-62:
(9*1)+(8*3)+(7*1)+(6*1)+(5*1)+(4*0)+(3*9)+(2*6)+(1*2)=92
92 % 10 = 2
So 1311109-62-2 is a valid CAS Registry Number.

1311109-62-2Relevant articles and documents

Ortho-(1-phenylvinyl)benzoate glycosylation donor, and preparation method and application thereof

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Paragraph 0103; 0107; 0169-0170; 0181-0182, (2020/05/01)

The invention discloses an ortho-(1-phenylvinyl)benzoate glycosylation donor, and a preparation method and an application thereof in a glycosylation reaction. The ortho-(1-phenylvinyl)benzoate glycosylation donor is stable, is easy to prepare and store, and is widely applied to the construction of various oxygen glucosides and nucleoside (nitrogen glucoside) glycosidic bonds. The leaving group ofthe donor is an alkenyl ester, has a high activity, and can be combined with thioglycoside or n-pentenyl ether glucoside through a one-pot glycosylation reaction to synthesize oligosaccharide. The glycosylation reaction conditions are mild, and receptors sensitive to acid and electrophilic reagents can tolerate the glycosylation reaction conditions.

An efficient approach to the synthesis of nucleosides: Gold(I)-catalyzed N-glycosylation of pyrimidines and purines with glycosyl ortho-alkynyl benzoates

Zhang, Qingju,Sun, Jiansong,Zhu, Yugen,Zhang, Fuyi,Yu, Biao

supporting information; experimental part, p. 4933 - 4936 (2011/06/24)

Persuaded with gold: The title reaction in the presence of [Ph 3PAuNTf2] (Tf=trifluoromethanesulfonyl) led conveniently to the corresponding nucleosides with excellent regioselectivity (see scheme). Even purine derivatives underwent this transformation owing to the mild conditions, which enabled the use of protecting groups that would not usually be compatible with N-glycosylation conditions. Copyright

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