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CAS

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868696-20-2

Butanedioic acid, mono[3-(1-phenylethenyl)-1,2,5-trioxaspiro[5.5]undec-9-yl] ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 868696-20-2 Structure

  • Basic information

    1. Product Name: Butanedioic acid, mono[3-(1-phenylethenyl)-1,2,5-trioxaspiro[5.5]undec-9-yl] ester
    2. Synonyms:
    3. CAS NO:868696-20-2
    4. Molecular Formula: C20H24O7
    5. Molecular Weight: 376.406
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 868696-20-2.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: Butanedioic acid, mono[3-(1-phenylethenyl)-1,2,5-trioxaspiro[5.5]undec-9-yl] ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Butanedioic acid, mono[3-(1-phenylethenyl)-1,2,5-trioxaspiro[5.5]undec-9-yl] ester(868696-20-2)
    11. EPA Substance Registry System: Butanedioic acid, mono[3-(1-phenylethenyl)-1,2,5-trioxaspiro[5.5]undec-9-yl] ester(868696-20-2)

  • 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: 868696-20-2(Hazardous Substances Data)

868696-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 868696-20-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,6,9 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 868696-20:
(8*8)+(7*6)+(6*8)+(5*6)+(4*9)+(3*6)+(2*2)+(1*0)=242
242 % 10 = 2
So 868696-20-2 is a valid CAS Registry Number.

868696-20-2Relevant articles and documents

New orally active spiro 1,2,4-trioxanes with high antimalarial potency

Singh, Chandan,Malik, Heetika,Puri, Sunil K.

, p. 4484 - 4487 (2005)

A new series of functionalized 1,2,4-trioxanes 10-21 have been prepared and assessed for antimalarial activity in mice. Several of these trioxanes show significant activity. Trioxane 16, the most active compound of the series, has shown activity by oral r

Orally active 1,2,4-trioxanes: Synthesis and antimalarial assessment of a new series of 9-functionalized 3-(1-arylvinyl)-1,2,5-trioxaspiro[5.5]undecanes against multi-drug-resistant Plasmodium yoelii nigeriensis in mice

Singh, Chandan,Malik, Heetika,Puri, Sunil K.

, p. 2794 - 2803 (2007/10/03)

Using easily accessible keto-trioxanes 7a-g as the starting materials, a series of new variously functionalized 1,2,4-trioxanes 10-36 have been prepared and evaluated for antimalarial activity against multi-drug-resistant Plasmodium yoelii nigeriensis in

Protection of the carbonyl group as 1,2,4-trioxane and its regeneration under basic conditions

Singh, Chandan,Malik, Heetika

, p. 5673 - 5676 (2007/10/03)

(Chemical Equation Presented) An experimental protocol demonstrating the protection of the carbonyl group as 1,2,4-trioxane, the stability of the protecting group under a variety of reaction conditions, and the regeneration of the carbonyl group with Triton B in THF at room temperature is presented. The method provides a useful alternative for the protection of carbonyl compounds having acid-sensitive moieties.

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