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129375-07-1

3-methyl-4-(1-methylethyl)phenyl 4-methoxybenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 129375-07-1 Structure

  • Basic information

    1. Product Name: 3-methyl-4-(1-methylethyl)phenyl 4-methoxybenzoate
    2. Synonyms: 3-methyl-4-(1-methylethyl)phenyl 4-methoxybenzoate
    3. CAS NO:129375-07-1
    4. Molecular Formula:
    5. Molecular Weight: 284.355
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 129375-07-1.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: 3-methyl-4-(1-methylethyl)phenyl 4-methoxybenzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-methyl-4-(1-methylethyl)phenyl 4-methoxybenzoate(129375-07-1)
    11. EPA Substance Registry System: 3-methyl-4-(1-methylethyl)phenyl 4-methoxybenzoate(129375-07-1)

  • 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: 129375-07-1(Hazardous Substances Data)

129375-07-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129375-07-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,3,7 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 129375-07:
(8*1)+(7*2)+(6*9)+(5*3)+(4*7)+(3*5)+(2*0)+(1*7)=141
141 % 10 = 1
So 129375-07-1 is a valid CAS Registry Number.

129375-07-1Relevant articles and documents

Lewis Acids Catalysed Fries Rearrangement of Isopropylcresol Esters

Martin, Robert,Demerseman, Pierre

, p. 227 - 236 (2007/10/02)

In the course of the Fries rearrangement, aluminium chloride frequently induces migration or elimination of alkyl groups.The results obtained with titanium tetrachloride for the synthesis of vicinal o-hydroxyketones are compared with those obtained with aluminium chloride for some aliphatic and aromatic esters of isopropylcresols.In order to understand the migration and elimination processes occurring, the stabilities of the o-hydroxyketones are studied in the presence of aluminium chloride at different temperatures.Furthermore, all-vicinal o-hydroxyketones were prepared by the Fries rearrangement of 6-tert-butyl-p-thymol with titanium tetrachloride.

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