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1372702-72-1

C18H16F2O5 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1372702-72-1 Structure

  • Basic information

    1. Product Name: C18H16F2O5
    2. Synonyms:
    3. CAS NO:1372702-72-1
    4. Molecular Formula:
    5. Molecular Weight: 350.319
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1372702-72-1.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: C18H16F2O5(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H16F2O5(1372702-72-1)
    11. EPA Substance Registry System: C18H16F2O5(1372702-72-1)

  • 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: 1372702-72-1(Hazardous Substances Data)

1372702-72-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1372702-72-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,2,7,0 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1372702-72:
(9*1)+(8*3)+(7*7)+(6*2)+(5*7)+(4*0)+(3*2)+(2*7)+(1*2)=151
151 % 10 = 1
So 1372702-72-1 is a valid CAS Registry Number.

1372702-72-1Relevant articles and documents

Oroxylin A analogs exhibited strong inhibitory activities against iNOS-mediated nitric oxide (NO) production

Pham, Tuan-Ahn. N.,Che, Haiyan,Phan, Phuong-Thuy T.,Lee, Jae-Won,Kim, Sung-Soo,Park, Haeil

, p. 2534 - 2535 (2012)

A number of oroxylin A analogs were prepared and evaluated for their inhibitory activities against iNOS-mediated nitric oxide (NO) production from LPS-stimulated BV2 cells. The analogs were synthesized from purchased 2′-hydroxy-4,5,6-trimethoxyacetophenone and aldehydes in 3 steps. Among the tested compounds, several analogs (3b, 3c, 3d, 3f) exhibited strong inhibitory activities. Especially, the analog with 4-nitrophenyl group (3b) showed stronger inhibitory activity (IC50 = 4.73 μM) than that of wogonin (IC50 = 7.80 μM).

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