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CAS

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1021462-11-2

2-(2,3,4-tri-O-acetyl-6-O-benzoyl-β-D-galactopyranosyl)-1,4-dimethoxynNphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1021462-11-2 Structure

  • Basic information

    1. Product Name: 2-(2,3,4-tri-O-acetyl-6-O-benzoyl-β-D-galactopyranosyl)-1,4-dimethoxynNphthalene
    2. Synonyms: 2-(2,3,4-tri-O-acetyl-6-O-benzoyl-β-D-galactopyranosyl)-1,4-dimethoxynNphthalene
    3. CAS NO:1021462-11-2
    4. Molecular Formula:
    5. Molecular Weight: 580.588
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1021462-11-2.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: 2-(2,3,4-tri-O-acetyl-6-O-benzoyl-β-D-galactopyranosyl)-1,4-dimethoxynNphthalene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2,3,4-tri-O-acetyl-6-O-benzoyl-β-D-galactopyranosyl)-1,4-dimethoxynNphthalene(1021462-11-2)
    11. EPA Substance Registry System: 2-(2,3,4-tri-O-acetyl-6-O-benzoyl-β-D-galactopyranosyl)-1,4-dimethoxynNphthalene(1021462-11-2)

  • 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: 1021462-11-2(Hazardous Substances Data)

1021462-11-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1021462-11-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,1,4,6 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1021462-11:
(9*1)+(8*0)+(7*2)+(6*1)+(5*4)+(4*6)+(3*2)+(2*1)+(1*1)=82
82 % 10 = 2
So 1021462-11-2 is a valid CAS Registry Number.

1021462-11-2Relevant articles and documents

Synthesis of β-C-glycopyranosyl-1,4-naphthoquinone derivatives and their cytotoxic activity

Lin, Li,He, Xiao-Peng,Xu, Qing,Chen, Guo-Rong,Xie, Juan

, p. 773 - 779 (2008/09/21)

β-C-Glucosyl and β-C-galactosyl-1,4-dimethoxynaphthalenes have been synthesized using a F3CCO2Ag/SnCl4 promoted Friedel-Crafts electrophilic substitution reaction. Both glycosyl acetates and methyl glycosides can be used as glycosyl donors. Further oxidation afforded the corresponding β-C-glycosyl-1,4-naphthoquinones. The in vitro cytotoxic activity of these compounds was evaluated against the A375 cell line.

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