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52309-82-7

4′-O-benzylapigenin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 52309-82-7 Structure

  • Basic information

    1. Product Name: 4′-O-benzylapigenin
    2. Synonyms: 4′-O-benzylapigenin
    3. CAS NO:52309-82-7
    4. Molecular Formula:
    5. Molecular Weight: 360.366
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 52309-82-7.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′-O-benzylapigenin(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4′-O-benzylapigenin(52309-82-7)
    11. EPA Substance Registry System: 4′-O-benzylapigenin(52309-82-7)

  • 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: 52309-82-7(Hazardous Substances Data)

52309-82-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52309-82-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,3,0 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 52309-82:
(7*5)+(6*2)+(5*3)+(4*0)+(3*9)+(2*8)+(1*2)=107
107 % 10 = 7
So 52309-82-7 is a valid CAS Registry Number.

52309-82-7Relevant articles and documents

Semisynthesis of apigenin and acacetin-7-O-β-d-glycosides from naringin and their cytotoxic activities

Liu, Jidan,Chen, Ling,Cai, Shuanglian,Wang, Qiuan

, p. 41 - 46 (2012/09/21)

Apigenin-7-O-β-d-glycosides 1-8 and acacetin-7-O-β-d-glycosides 9-16 were semisynthesized from 4′-O-benzyl apigenin 17 and acacetin 18 by glycosidation and deprotection with the corresponding α-acetylglycosyl bromide, respectively. Compounds 17 and 18 were prepared by iodination followed by base-induced elimination, 4′-O-benzylation, or 4′-O-methylation and acid hydrolysis using naringin as starting material which is readily available and cheap. Their cytotoxic potential against five human cancer cell lines (HL-60, SMMC-7721, A-549, MCF-7, and SW480) was evaluated by standard MTT method. The results show that compounds 2, 9, and 19 exhibit moderate cytotoxicity against HL-60, SMMC-7721, A-549, MCF-7, and SW480, while compound 3 exhibits potent cytotoxicity against MCF-7 selectively. Among the synthesized target compounds, 3, 4, 7, 11, 12, 15, and 16 were new compounds, the natural product 8 was the first synthesized and the synthesis of natural products 5, 6, 13, and 14 was efficiently improved by the new synthetic routes.

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