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4'-chloro-7-O-β-D-galactoside flavone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1209000-36-1 Structure
  • Basic information

    1. Product Name: 4'-chloro-7-O-β-D-galactoside flavone
    2. Synonyms: 4'-chloro-7-O-β-D-galactoside flavone
    3. CAS NO:1209000-36-1
    4. Molecular Formula:
    5. Molecular Weight: 434.83
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1209000-36-1.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: 4'-chloro-7-O-β-D-galactoside flavone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4'-chloro-7-O-β-D-galactoside flavone(1209000-36-1)
    11. EPA Substance Registry System: 4'-chloro-7-O-β-D-galactoside flavone(1209000-36-1)
  • 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: 1209000-36-1(Hazardous Substances Data)

1209000-36-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1209000-36-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,9,0,0 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1209000-36:
(9*1)+(8*2)+(7*0)+(6*9)+(5*0)+(4*0)+(3*0)+(2*3)+(1*6)=91
91 % 10 = 1
So 1209000-36-1 is a valid CAS Registry Number.

1209000-36-1Downstream Products

1209000-36-1Relevant articles and documents

Synthesis of flavonoid 7-O-β-D-glycosides by phase transfer catalysis

Wu, Zheng,Jiang, Ling,Chen, He,Wang, Qiu-An

, p. 195 - 197 (2009)

Six flavonoid 7-O-β-D-glycosides 1a-3a and 1b-3b were synthesised from the flavones 7a and 7b by glycosidation and deacetylation with the corresponding a-acetylglycosyl bromides. 7a and 7b were prepared in high yield by an improved Baker-Venkataraman rearrangement using 2, 4- dihydro×yacetophenone as starting material and tetrabutylammonium bromide (TBAB) as a phase transfer catalyst. The glycosidation procedure was modified by using anhydrous K2CO3 in a solvent mixture of DMF/acetone (3:2v/v) and TBAB as a phase transfer catalyst.

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