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76480-04-1

4-Isobutoxy-benzoic acid isobutyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76480-04-1 Structure

  • Basic information

    1. Product Name: 4-Isobutoxy-benzoic acid isobutyl ester
    2. Synonyms: 4-Isobutoxy-benzoic acid isobutyl ester
    3. CAS NO:76480-04-1
    4. Molecular Formula:
    5. Molecular Weight: 250.338
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76480-04-1.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: 4-Isobutoxy-benzoic acid isobutyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Isobutoxy-benzoic acid isobutyl ester(76480-04-1)
    11. EPA Substance Registry System: 4-Isobutoxy-benzoic acid isobutyl ester(76480-04-1)

  • 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: 76480-04-1(Hazardous Substances Data)

76480-04-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76480-04-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,4,8 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76480-04:
(7*7)+(6*6)+(5*4)+(4*8)+(3*0)+(2*0)+(1*4)=141
141 % 10 = 1
So 76480-04-1 is a valid CAS Registry Number.

76480-04-1Downstream Products

76480-04-1Relevant articles and documents

Competing SNAr displacements of nitrite and SN2 displacements on the alkyl groups of alkyl p-nitrobenzoates and o-nitrobenzoates

Logue, Marshall W.,Han, Byung Hee

, p. 1638 - 1642 (1981)

Several p-nitrobenzoate and o-nitrobenzoate esters have been found to undergo competing SNAr and SN2 reactions with azide, alkoxide, and thiophenoxide ions. SNAr displacement of the nitro group even competes with SN2 displacement on the methyl group of methyl esters 1c and 11. Esters 1a and 1b undergo predominately SNAr displacements with azide, whereas 1c undergoes predominately an SN2 displacement with azide. Both 1b and 1c undergo predominately SNAr reactions with alkoxides and thiophenoxide. The SNAr products from the azide reactions consist of mixtures of p-azidobenzoates, p-aminobenzoates, and 4,4′-azodibenzoates whose compositions depend upon the reaction conditions.

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