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444313-77-3

C1-13C-tri-O-benzyl-D-glucal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 444313-77-3 Structure

  • Basic information

    1. Product Name: C1-13C-tri-O-benzyl-D-glucal
    2. Synonyms: C1-13C-tri-O-benzyl-D-glucal
    3. CAS NO:444313-77-3
    4. Molecular Formula:
    5. Molecular Weight: 417.506
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 444313-77-3.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: C1-13C-tri-O-benzyl-D-glucal(CAS DataBase Reference)
    10. NIST Chemistry Reference: C1-13C-tri-O-benzyl-D-glucal(444313-77-3)
    11. EPA Substance Registry System: C1-13C-tri-O-benzyl-D-glucal(444313-77-3)

  • 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: 444313-77-3(Hazardous Substances Data)

444313-77-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 444313-77-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,4,3,1 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 444313-77:
(8*4)+(7*4)+(6*4)+(5*3)+(4*1)+(3*3)+(2*7)+(1*7)=133
133 % 10 = 3
So 444313-77-3 is a valid CAS Registry Number.

444313-77-3Downstream Products

444313-77-3Relevant articles and documents

C2-amidoglycosylation. Scope and mechanism of nitrogen transfer

Liu, Jing,Gin, David Y.

, p. 9789 - 9797 (2007/10/03)

A one-pot C2-amidoglycosylation reaction for the synthesis of 2-N-acyl-2-deoxy-β-pyranosides from glycals is described. Glycal donors activated by the reagent combination of thianthrene-5-oxide (11) and Tf2O, followed by treatment with an amide nucleophile and a glycosyl acceptor, lead to the formation of various C2-amidoglycoconjugates. Both the C2-nitrogen transfer and the glycosidic bond formation proceed stereoselectively, allowing for the introduction of both natural and nonnatural amide functionalities at C2 with concomitant anomeric bond formation in a one-pot procedure. Tracking of the reaction by low-temperature NMR spectroscopy employing 15N- and 18O-isotope labels suggests a mechanism involving the formation of the C2-sulfonium glycosyl imidate 39 as well as oxazoline 37 as key intermediates in this novel oxidative glycosylation process.

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