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73455-03-5

1,3-Benzodioxole, 5-(1-methoxypropyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 73455-03-5 Structure

  • Basic information

    1. Product Name: 1,3-Benzodioxole, 5-(1-methoxypropyl)-
    2. Synonyms:
    3. CAS NO:73455-03-5
    4. Molecular Formula: C11H14O3
    5. Molecular Weight: 194.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 73455-03-5.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: 1,3-Benzodioxole, 5-(1-methoxypropyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3-Benzodioxole, 5-(1-methoxypropyl)-(73455-03-5)
    11. EPA Substance Registry System: 1,3-Benzodioxole, 5-(1-methoxypropyl)-(73455-03-5)

  • 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: 73455-03-5(Hazardous Substances Data)

73455-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73455-03-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,4,5 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73455-03:
(7*7)+(6*3)+(5*4)+(4*5)+(3*5)+(2*0)+(1*3)=125
125 % 10 = 5
So 73455-03-5 is a valid CAS Registry Number.

73455-03-5Relevant articles and documents

Palladium charcoal-catalyzed deprotection of O-allylphenols

Ishizaki, Miyuki,Yamada, Makoto,Watanabe, Shin-Ichi,Hoshino, Osamu,Nishitani, Kiyoshi,Hayashida, Maiko,Tanaka, Atsuko,Hara, Hiroshi

, p. 7973 - 7981 (2007/10/03)

Allyl aryl ethers can be easily cleaved by the use of 10% Pd/C under mild and basic conditions. The present reaction would involve a SET process rather than a π-allyl-palladium complex. The scope and limitation of this new deprotective methodology is also described.

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