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1403563-07-4

C16H14Cl2O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1403563-07-4 Structure

  • Basic information

    1. Product Name: C16H14Cl2O
    2. Synonyms:
    3. CAS NO:1403563-07-4
    4. Molecular Formula:
    5. Molecular Weight: 293.193
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1403563-07-4.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: C16H14Cl2O(CAS DataBase Reference)
    10. NIST Chemistry Reference: C16H14Cl2O(1403563-07-4)
    11. EPA Substance Registry System: C16H14Cl2O(1403563-07-4)

  • 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: 1403563-07-4(Hazardous Substances Data)

1403563-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1403563-07-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,3,5,6 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1403563-07:
(9*1)+(8*4)+(7*0)+(6*3)+(5*5)+(4*6)+(3*3)+(2*0)+(1*7)=124
124 % 10 = 4
So 1403563-07-4 is a valid CAS Registry Number.

1403563-07-4Downstream Products

1403563-07-4Relevant articles and documents

Synthesis and antimalarial activity of 3,3-spiroanellated 5,6-disubstituted 1,2,4-trioxanes

Maurya, Ranjani,Soni, Awakash,Anand, Devireddy,Ravi, Makthala,Raju, Kanumuri S.R.,Taneja, Isha,Naikade, Niraj K.,Puri,Wahajuddin,Kanojiya, Sanjeev,Yadav, Prem P.

, p. 165 - 169 (2013/03/29)

Novel 3,3-spiroanellated 5-aryl, 6-arylvinyl-substituted 1,2,4-trioxanes 19-34 have been synthesized and appraised for their antimalarial activity against multidrug-resistant Plasmodium yoelii nigeriensis in Swiss mice by oral route at doses ranging from 96 mg/kg × 4 days to 24 mg/kg × 4 days. The most active compound of the series (compound 25) provided 100% protection at 24 mg/kg × 4 days, and other 1,2,4-trioxanes 22, 26, 27, and 30 also showed promising activity. In this model, β-arteether provided 100 and 20% protection at 48 mg/kg × 4 days and 24 mg/kg × 4 days, respectively, by oral route. Compound 25 displayed a similar in vitro pharmacokinetic profile to that of reference drug β-arteether. The activity results demonstrated the importance of an aryl moiety at the C-5 position on the 1,2,4-trioxane pharmacophore.

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