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4-methylphenyl 3,4,5-trimethoxybenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 129194-52-1 Structure
  • Basic information

    1. Product Name: 4-methylphenyl 3,4,5-trimethoxybenzoate
    2. Synonyms: 4-methylphenyl 3,4,5-trimethoxybenzoate
    3. CAS NO:129194-52-1
    4. Molecular Formula: C17H18O5
    5. Molecular Weight: 302.32
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 129194-52-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-methylphenyl 3,4,5-trimethoxybenzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-methylphenyl 3,4,5-trimethoxybenzoate(129194-52-1)
    11. EPA Substance Registry System: 4-methylphenyl 3,4,5-trimethoxybenzoate(129194-52-1)
  • 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: 129194-52-1(Hazardous Substances Data)

129194-52-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129194-52-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,1,9 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 129194-52:
(8*1)+(7*2)+(6*9)+(5*1)+(4*9)+(3*4)+(2*5)+(1*2)=141
141 % 10 = 1
So 129194-52-1 is a valid CAS Registry Number.

129194-52-1Downstream Products

129194-52-1Relevant articles and documents

N-heterocyclic carbenes: IX. Oxidative esterification of aromatic aldehydes with arylboronic acids catalyzed by N-heterocyclic carbenes

Denisov,Gorbunov,Glushkov

, p. 86 - 90 (2015/03/04)

Aromatic aldehydes reacted with arylboronic acids under catalysis by N-heterocyclic carbene and oxic conditions to produce phenol esters.

Polar Effects in the Decomposition of Bis(3-alkoxyaroyl) Peroxides. Synthesis of 8-Alkoxy-6H-dibenzopyran-6-ones

Auricchio, Sergio,Citterio, Attilio,Sebastiano, Roberto

, p. 6312 - 6316 (2007/10/02)

The reaction of four substituted bis(3-alkoxybenzoyl) peroxides (1b-e) in neat phenols (2a-e) affords mainly 8-alkoxy-6H-dibenzopyran-6-ones (7) and ortho-benzoyloxylation products (4) of the phenol.Diaroyl peroxides without electron-releasing meta substituents afford essentially products 4.A mechanism involving monoelectronic oxidation of the phenol by the peroxide and biaryl coupling by preferential addition of the phenol radical cation to the ortho positions to the alkoxy group of the diaroyl peroxide is suggested.

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