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1450665-53-8

8-chloro-3-[2-(3-nitrophenyl)hydrazono]quinoline-2,4-(1H,3H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1450665-53-8 Structure

  • Basic information

    1. Product Name: 8-chloro-3-[2-(3-nitrophenyl)hydrazono]quinoline-2,4-(1H,3H)-dione
    2. Synonyms: 8-chloro-3-[2-(3-nitrophenyl)hydrazono]quinoline-2,4-(1H,3H)-dione
    3. CAS NO:1450665-53-8
    4. Molecular Formula:
    5. Molecular Weight: 344.714
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1450665-53-8.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: 8-chloro-3-[2-(3-nitrophenyl)hydrazono]quinoline-2,4-(1H,3H)-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 8-chloro-3-[2-(3-nitrophenyl)hydrazono]quinoline-2,4-(1H,3H)-dione(1450665-53-8)
    11. EPA Substance Registry System: 8-chloro-3-[2-(3-nitrophenyl)hydrazono]quinoline-2,4-(1H,3H)-dione(1450665-53-8)

  • 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: 1450665-53-8(Hazardous Substances Data)

1450665-53-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1450665-53-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,0,6,6 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1450665-53:
(9*1)+(8*4)+(7*5)+(6*0)+(5*6)+(4*6)+(3*5)+(2*5)+(1*3)=158
158 % 10 = 8
So 1450665-53-8 is a valid CAS Registry Number.

1450665-53-8Downstream Products

1450665-53-8Relevant articles and documents

Synthesis and binary QSAR study of antitubercular quinolylhydrazides

Manvar, Atul,Khedkar, Vijay,Patel, Jignesh,Vora, Vipul,Dodia, Narsinh,Patel, Gautam,Coutinho, Evans,Shah, Anamik

, p. 4896 - 4902 (2013)

In continuation with our previous work in anti-TB research area, in the present study we have demonstrated the structural diversity of quinolylhydrazides as potent anti-tuberculars. The compound library was synthesized by molecular hybridization approach and tested in vitro against Mycobacterium tuberculosis H37Rv strains. Among the designed conjugates, the most promising molecules were found to exhibit 100% Growth Inhibition (GI) at MIC 6.25 μg/mL. Moreover, several analogs in the designed series were also turned out as excellent anti-tuberculars. To probe the structural characteristics influencing on the SAR, the classification model was generated using a binary QSAR approach termed recursive partitioning (RP) analysis. The significant features outlined by the RP model act as a guide in order to design the 'lead' compound.

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