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CAS

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1454839-26-9

S-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-2,3-dichlorophenylthiohydroxamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1454839-26-9 Structure

  • Basic information

    1. Product Name: S-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-2,3-dichlorophenylthiohydroxamate
    2. Synonyms: S-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-2,3-dichlorophenylthiohydroxamate
    3. CAS NO:1454839-26-9
    4. Molecular Formula:
    5. Molecular Weight: 552.386
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1454839-26-9.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: S-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-2,3-dichlorophenylthiohydroxamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: S-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-2,3-dichlorophenylthiohydroxamate(1454839-26-9)
    11. EPA Substance Registry System: S-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-2,3-dichlorophenylthiohydroxamate(1454839-26-9)

  • 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: 1454839-26-9(Hazardous Substances Data)

1454839-26-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1454839-26-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,4,8,3 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1454839-26:
(9*1)+(8*4)+(7*5)+(6*4)+(5*8)+(4*3)+(3*9)+(2*2)+(1*6)=189
189 % 10 = 9
So 1454839-26-9 is a valid CAS Registry Number.

1454839-26-9Relevant articles and documents

Preparation and X-ray analysis of potassium (2,3-dichlorophenyl) glucosinolate

Vo, Quan V.,Trenerry, Craige,Rochfort, Simone,White, Jonathan,Hughes, Andrew B.

, p. 588 - 594 (2014/08/18)

There has been much interest in obtaining crystals for crystallographic analysis of biologically active glucosinolates. Crystals of potassium (2,3-dichlorophenyl)glucosinolate were obtained as a dual solvate, containing one methanol and one ethanol molecule of crystallization, K+ C 13H14Cl2NO9S2 - CH3OH C2H5OH. The three-dimensional polymeric network consists of chains containing the potassium ions coordinated and bridged by sugar O atoms, which run parallel to the a axis and are further crosslinked through the sugar molecules. The channels of this network are occupied by the dichlorophenyl substituents and the ethanol and methanol solvent molecules. The structure of the S-(2,3,4,6-tetra-O-acetyl- β-d-glucopyranosyl)-2,3-dichlorophenylacetothiohydroxymate, C 21H23Cl2NO10S, precursor has also been determined and the β-configuration and Z isomer of the thiohydroximate substituent is confirmed.

Synthesis and anti-inflammatory activity of aromatic glucosinolates

Vo, Quan V.,Trenerry, Craige,Rochfort, Simone,Wadeson, Jenny,Leyton, Carolina,Hughes, Andrew B.

, p. 5945 - 5954 (2013/09/23)

Aromatic GLs are important members of the glucosinolate family of compounds because of their potential biological activity and medicinal properties. This study has shown success in the high yielding synthesis of some important aromatic GLs as well as the results of testing for anti-inflammatory properties of the synthetic GLs. 3,4-Dimethoxyphenylglucosinolate was found to be the most active anti-inflammatory of the seven glucosinolates assayed.

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