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benzyl 4-methoxybenzyl phthalate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1575722-30-3 Structure
  • Basic information

    1. Product Name: benzyl 4-methoxybenzyl phthalate
    2. Synonyms: benzyl 4-methoxybenzyl phthalate
    3. CAS NO:1575722-30-3
    4. Molecular Formula:
    5. Molecular Weight: 376.409
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1575722-30-3.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: benzyl 4-methoxybenzyl phthalate(CAS DataBase Reference)
    10. NIST Chemistry Reference: benzyl 4-methoxybenzyl phthalate(1575722-30-3)
    11. EPA Substance Registry System: benzyl 4-methoxybenzyl phthalate(1575722-30-3)
  • 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: 1575722-30-3(Hazardous Substances Data)

1575722-30-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1575722-30-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,5,7,2 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1575722-30:
(9*1)+(8*5)+(7*7)+(6*5)+(5*7)+(4*2)+(3*2)+(2*3)+(1*0)=183
183 % 10 = 3
So 1575722-30-3 is a valid CAS Registry Number.

1575722-30-3Downstream Products

1575722-30-3Relevant articles and documents

Proton-exchanged montmorillonite-mediated reactions of methoxybenzyl esters and ethers

Chen, Dongyin,Xu, Chang,Deng, Jie,Jiang, Chunhuan,Wen, Xiaoan,Kong, Lingyi,Zhang, Ji,Sun, Hongbin

supporting information, p. 1975 - 1983 (2014/03/21)

Proton-exchanged montmorillonite (H-mont) was found to be an eco-friendly and cost-effective catalyst for the generation of O-methylated quinone methides (QM) from the corresponding p or o-methoxybenzyl esters and ethers. Nucleophilic trapping of the O-methylated QM with arenes, alcohols, 1,3-dicarbonyl compounds, silyl enol ethers, and allylsilanes has been carried out, respectively, leading to eco-friendly benzylation reactions. Using this protocol, H-mont-mediated deprotection of PMB-protected esters and ethers have been realized for the first time. This work would pave the way for further exploration in O-alkylated QM that are of chemical and biological significance.

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