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CAS

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124549-64-0

(RS)-3-butyl-4,5,6,7-tetrahydroisobenzofuran-1(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124549-64-0 Structure

  • Basic information

    1. Product Name: (RS)-3-butyl-4,5,6,7-tetrahydroisobenzofuran-1(3H)-one
    2. Synonyms:
    3. CAS NO:124549-64-0
    4. Molecular Formula:
    5. Molecular Weight: 194.274
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124549-64-0.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: (RS)-3-butyl-4,5,6,7-tetrahydroisobenzofuran-1(3H)-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (RS)-3-butyl-4,5,6,7-tetrahydroisobenzofuran-1(3H)-one(124549-64-0)
    11. EPA Substance Registry System: (RS)-3-butyl-4,5,6,7-tetrahydroisobenzofuran-1(3H)-one(124549-64-0)

  • 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: 124549-64-0(Hazardous Substances Data)

124549-64-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124549-64-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,5,4 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 124549-64:
(8*1)+(7*2)+(6*4)+(5*5)+(4*4)+(3*9)+(2*6)+(1*4)=130
130 % 10 = 0
So 124549-64-0 is a valid CAS Registry Number.

124549-64-0Downstream Products

124549-64-0Relevant articles and documents

Total syntheses of (±)-cis- and (±)-trans-neocnidilides

Mahadevegowda, Surendra H.,Khan, Faiz Ahmed

, p. 4400 - 4403 (2014)

Total syntheses of two antimicrobial natural products (±)-cis- neocnidilide and (±)-trans-neocnidilide starting from a readily preparable cyclohexa[b]-fused 5-oxabicyclo[2.1.1]hexane derivative are presented. The diastereomeric tetrahydrofuran tricarboxylate epimers obtained from a BF3·OEt2 promoted Grob-type fragmentation of the oxa-bicycle derivative were converted into title natural products by employing pyridinium dichromate/acetic anhydride mediated bis-oxidative cleavage reaction.

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