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CAS

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153908-85-1

5-[(E)-3-Methyl-5-((S)-2,2,5,5-tetramethyl-[1,3]dioxolan-4-yl)-pent-2-enyloxy]-benzo[1,3]dioxole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 153908-85-1 Structure

  • Basic information

    1. Product Name: 5-[(E)-3-Methyl-5-((S)-2,2,5,5-tetramethyl-[1,3]dioxolan-4-yl)-pent-2-enyloxy]-benzo[1,3]dioxole
    2. Synonyms:
    3. CAS NO:153908-85-1
    4. Molecular Formula:
    5. Molecular Weight: 348.439
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 153908-85-1.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: 5-[(E)-3-Methyl-5-((S)-2,2,5,5-tetramethyl-[1,3]dioxolan-4-yl)-pent-2-enyloxy]-benzo[1,3]dioxole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-[(E)-3-Methyl-5-((S)-2,2,5,5-tetramethyl-[1,3]dioxolan-4-yl)-pent-2-enyloxy]-benzo[1,3]dioxole(153908-85-1)
    11. EPA Substance Registry System: 5-[(E)-3-Methyl-5-((S)-2,2,5,5-tetramethyl-[1,3]dioxolan-4-yl)-pent-2-enyloxy]-benzo[1,3]dioxole(153908-85-1)

  • 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: 153908-85-1(Hazardous Substances Data)

153908-85-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153908-85-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,9,0 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 153908-85:
(8*1)+(7*5)+(6*3)+(5*9)+(4*0)+(3*8)+(2*8)+(1*5)=151
151 % 10 = 1
So 153908-85-1 is a valid CAS Registry Number.

153908-85-1Relevant articles and documents

Microbiological transformation. 30. Enantioselective hydrolysis of racemic epoxides: The synthesis of enantiopure insect juvenile hormone analogs (Bower's compound)

Archelas,Delbecque,Furstoss

, p. 2445 - 2446 (2007/10/02)

The enantioselective epoxide biohydrolysis of the racemic benzodioxole 6,7-epoxygeraniol derivative 1 has been achieved using the fungus A. niger. This new type of preparative scale bioconversion allows the synthesis of both enantiomers of Bower's compound, an analogue of insect juvenile hormone. Biological tests showed that the 6(R) enantiomer was about ten times more active than the 6(S) enantiomer against the yellow meal worm Tenebrio molitor.

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