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82467-94-5

1(3H)-Isobenzofuranone,3-butyl-4,5-dihydro-,(3R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 82467-94-5 Structure

  • Basic information

    1. Product Name: 1(3H)-Isobenzofuranone,3-butyl-4,5-dihydro-,(3R)-
    2. Synonyms:
    3. CAS NO:82467-94-5
    4. Molecular Formula:
    5. Molecular Weight:
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 82467-94-5.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(3H)-Isobenzofuranone,3-butyl-4,5-dihydro-,(3R)- (CAS DataBase Reference)
    10. NIST Chemistry Reference: 1(3H)-Isobenzofuranone,3-butyl-4,5-dihydro-,(3R)- (82467-94-5)
    11. EPA Substance Registry System: 1(3H)-Isobenzofuranone,3-butyl-4,5-dihydro-,(3R)- (82467-94-5)

  • 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: 82467-94-5(Hazardous Substances Data)

82467-94-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82467-94-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,4,6 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82467-94:
(7*8)+(6*2)+(5*4)+(4*6)+(3*7)+(2*9)+(1*4)=155
155 % 10 = 5
So 82467-94-5 is a valid CAS Registry Number.

82467-94-5Downstream Products

82467-94-5Relevant articles and documents

Asymmetric synthesis and sensory evaluation of sedanenolide

Oguro, Daichi,Watanabe, Hidenori

, p. 1502 - 1505 (2011)

The synthesis and sensory evaluation of enantiomeric sets of sedanenolide (1) and 3-butylphthalide (3) are described. The asymmetric synthesis was achieved via the intramolecular Diels-Alder reaction of chiral propargylester (5) which was prepared from optically active propargyl alcohol (4) and 2,4-pentadienoic acid. The sensory evaluation of these enantiomers revealed that there were distinct differences between their aroma character and odor threshold.

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