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CAS

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651736-01-5

methyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-allopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 651736-01-5 Structure

  • Basic information

    1. Product Name: methyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-allopyranoside
    2. Synonyms: methyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-allopyranoside
    3. CAS NO:651736-01-5
    4. Molecular Formula:
    5. Molecular Weight: 281.309
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 651736-01-5.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: methyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-allopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-allopyranoside(651736-01-5)
    11. EPA Substance Registry System: methyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-allopyranoside(651736-01-5)

  • 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: 651736-01-5(Hazardous Substances Data)

651736-01-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 651736-01-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,1,7,3 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 651736-01:
(8*6)+(7*5)+(6*1)+(5*7)+(4*3)+(3*6)+(2*0)+(1*1)=155
155 % 10 = 5
So 651736-01-5 is a valid CAS Registry Number.

651736-01-5Relevant articles and documents

A comparative study of the O-3 reactivity of isomeric N-dimethylmaleoyl- protected d-glucosamine and d-allosamine acceptors

Colombo, María I.,Stortz, Carlos A.,Rúveda, Edmundo A.

experimental part, p. 569 - 576 (2011/05/04)

Four isomeric N-dimethylmaleoyl 4,6-O-benzylidene-protected d-hexosamine acceptors (2, 3, 4, and 5) with all possible configurations at C-1 and C-3 (e.g., derived from d-glucosamine and d-allosamine) were prepared, and the assessment of their O-3 relative

Precise structure activity relationships in asymmetric catalysis using carbohydrate scaffolds to allow ready fine tuning: dialkylzinc-aldehyde additions.

Emmerson, Daniel P G,Villard, Renaud,Mugnaini, Claudia,Batsanov, Andrei,Howard, Judith A K,Hems, William P,Tooze, Robert P,Davis, Benjamin G

, p. 3826 - 3838 (2007/10/03)

The ready construction of 24 stereochemically and functionally diverse carbohydrate ligand structures from a core D-glucosamine scaffold has allowed the evaluation of broad ranging structure activity relationships in ligand accelerated zincate additions t

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