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1101829-31-5

C18H26O3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1101829-31-5 Structure

  • Basic information

    1. Product Name: C18H26O3
    2. Synonyms:
    3. CAS NO:1101829-31-5
    4. Molecular Formula:
    5. Molecular Weight: 290.403
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1101829-31-5.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: C18H26O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H26O3(1101829-31-5)
    11. EPA Substance Registry System: C18H26O3(1101829-31-5)

  • 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: 1101829-31-5(Hazardous Substances Data)

1101829-31-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1101829-31-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,1,8,2 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1101829-31:
(9*1)+(8*1)+(7*0)+(6*1)+(5*8)+(4*2)+(3*9)+(2*3)+(1*1)=105
105 % 10 = 5
So 1101829-31-5 is a valid CAS Registry Number.

1101829-31-5Downstream Products

1101829-31-5Relevant articles and documents

Synthesis of spiro-1,2-dioxolanes and their activity against Plasmodium falciparum

Martyn, Derek C.,Ramirez, Armando P.,Beattie, Meaghan J.,Cortese, Joseph F.,Patel, Vishal,Rush, Margaret A.,Woerpel,Clardy, Jon

, p. 6521 - 6524 (2008)

Artemisinin-derived compounds play an integral role in current malaria chemotherapy. Given the virtual certainty of emerging resistance, we have investigated spiro-1,2-dioxolanes as an alternative scaffold. The endoperoxide functionality was generated by the SnCl4-mediated annulation of a bis-silylperoxide and an alkene. The first set of eight analogs gave EC50 values of 50-150 nM against Plasmodium falciparum 3D7 and Dd2 strains, except for the carboxylic acid analog. A second series, synthesized by coupling a spiro-1,2-dioxolane carboxylic acid to four separate amines, afforded the most potent compound (EC50 ～5 nM).

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