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7,8-dihydroxy-4'-trimethylsilylisoflavone 7-O-α-D-arabinofuranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1051923-41-1 Structure
  • Basic information

    1. Product Name: 7,8-dihydroxy-4'-trimethylsilylisoflavone 7-O-α-D-arabinofuranoside
    2. Synonyms: 7,8-dihydroxy-4'-trimethylsilylisoflavone 7-O-α-D-arabinofuranoside
    3. CAS NO:1051923-41-1
    4. Molecular Formula:
    5. Molecular Weight: 458.54
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1051923-41-1.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: 7,8-dihydroxy-4'-trimethylsilylisoflavone 7-O-α-D-arabinofuranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7,8-dihydroxy-4'-trimethylsilylisoflavone 7-O-α-D-arabinofuranoside(1051923-41-1)
    11. EPA Substance Registry System: 7,8-dihydroxy-4'-trimethylsilylisoflavone 7-O-α-D-arabinofuranoside(1051923-41-1)
  • 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: 1051923-41-1(Hazardous Substances Data)

1051923-41-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1051923-41-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,1,9,2 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1051923-41:
(9*1)+(8*0)+(7*5)+(6*1)+(5*9)+(4*2)+(3*3)+(2*4)+(1*1)=121
121 % 10 = 1
So 1051923-41-1 is a valid CAS Registry Number.

1051923-41-1Downstream Products

1051923-41-1Relevant articles and documents

Isoflavone glycosides: Synthesis and evaluation as α-glucosidase inhibitors

Wei, Guo,Yu, Biao

experimental part, p. 3156 - 3163 (2009/06/06)

On the basis of the structure of 4′,7,8-trihydroxyisoflavone 7-O-α-D-arabinofuranoside (namely A-76202, 1), a Rhodococcus metabolite showing potent inhibitory activities against the α-glucosidases of rat liver microsome (IC50 = 0.46 ng/mL), 26 analogs, each with minor variations at the sugar moiety and the isoflavone A and B rings, were readily synthesized. Notably, a new and efficient method was developed for the divergent synthesis of the B-ring congeners of the isoflavone glycosides by using Suzuki-Miyaura coupling as the final step. Modifications at the sugar moiety and the isoflavone A ring significantly diminish the activity, whereas variations at the B ring are largely tolerated for retaining the potent α-glucosidase inhibitory activity. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

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