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CAS

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868744-51-8

benzyl 2-acetamido-3,6-di-O-benzoyl-2-deoxy-β-D-galactopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 868744-51-8 Structure

  • Basic information

    1. Product Name: benzyl 2-acetamido-3,6-di-O-benzoyl-2-deoxy-β-D-galactopyranoside
    2. Synonyms: benzyl 2-acetamido-3,6-di-O-benzoyl-2-deoxy-β-D-galactopyranoside
    3. CAS NO:868744-51-8
    4. Molecular Formula:
    5. Molecular Weight: 519.551
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 868744-51-8.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: benzyl 2-acetamido-3,6-di-O-benzoyl-2-deoxy-β-D-galactopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: benzyl 2-acetamido-3,6-di-O-benzoyl-2-deoxy-β-D-galactopyranoside(868744-51-8)
    11. EPA Substance Registry System: benzyl 2-acetamido-3,6-di-O-benzoyl-2-deoxy-β-D-galactopyranoside(868744-51-8)

  • 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: 868744-51-8(Hazardous Substances Data)

868744-51-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 868744-51-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,7,4 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 868744-51:
(8*8)+(7*6)+(6*8)+(5*7)+(4*4)+(3*4)+(2*5)+(1*1)=228
228 % 10 = 8
So 868744-51-8 is a valid CAS Registry Number.

868744-51-8Relevant articles and documents

Investigating bacterial N-linked glycosylation: Synthesis and glycosyl acceptor activity of the undecaprenyl pyrophosphate-linked bacillosamine

Weerapana, Eranthie,Glover, Kerney Jebrell,Chen, Mark M.,Imperiali, Barbara

, p. 13766 - 13767 (2005)

The chemical synthesis and biological activity of undecaprenyl pyrophosphate bacillosamine (Und-PP-Bac), an obligatory intermediate in the asparagine-linked glycosylation pathway of Campylobacter jejuni, are reported. The key transformation involves the c

Chemoenzymatic Synthesis of 4-Fluoro-N-Acetylhexosamine Uridine Diphosphate Donors: Chain Terminators in Glycosaminoglycan Synthesis

Schultz, Victor L.,Zhang, Xing,Linkens, Kathryn,Rimel, Jenna,Green, Dixy E.,Deangelis, Paul L.,Linhardt, Robert J.

, p. 2243 - 2248 (2017/02/26)

Unnatural uridine diphosphate (UDP)-sugar donors, UDP-4-deoxy-4-fluoro-N-acetylglucosamine (4FGlcNAc) and UDP-4-deoxy-4-fluoro-N-acetylgalactosamine (4FGalNAc), were prepared using both chemical and chemoenzymatic syntheses relying on N-acetylglucosamine-

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