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1338561-42-4

C24H16ClF2NO3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1338561-42-4 Structure

  • Basic information

    1. Product Name: C24H16ClF2NO3
    2. Synonyms: C24H16ClF2NO3
    3. CAS NO:1338561-42-4
    4. Molecular Formula:
    5. Molecular Weight: 439.846
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1338561-42-4.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: C24H16ClF2NO3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C24H16ClF2NO3(1338561-42-4)
    11. EPA Substance Registry System: C24H16ClF2NO3(1338561-42-4)

  • 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: 1338561-42-4(Hazardous Substances Data)

1338561-42-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1338561-42-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,8,5,6 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1338561-42:
(9*1)+(8*3)+(7*3)+(6*8)+(5*5)+(4*6)+(3*1)+(2*4)+(1*2)=164
164 % 10 = 4
So 1338561-42-4 is a valid CAS Registry Number.

1338561-42-4Relevant articles and documents

Synthesis and biological evaluation of HQCAs with aryl or benzyl substituents on N-1 position as potential HIV-1 integrase inhibitors

He, Qiu-Qin,Zhang, Xuan,Wu, Hai-Qiu,Gu, Shuang-Xi,Ma, Xiao-Dong,Yang, Liu-Meng,Zheng, Yong-Tang,Chen, Fen-Er

, p. 5553 - 5558 (2011/10/19)

A series of new 5-hydroxylquinolone-3-carboxylic acids (HQCAs) with various aryl or benzyl substituents on N-1 position were synthesized and evaluated for their anti-HIV activity in C8166 cell culture. Most of the target compounds displayed activity against wide-type HIV-1 in the low micromolar range in infected C8166 cells. The most active compound 5g exhibited activity against wild-type HIV-1 and HIV-1 mutant virus A17 with an EC50 value of 3.17 and 17.88 μM, respectively. The biological results and the docking study revealed that the substitution pattern on N-1 position of the quinolone core might contribute to physicochemical properties of HQCAs and resulted in great influence on their antiviral potency.

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