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2,4-dimethoxyphenyl benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 18093-01-1 Structure
  • Basic information

    1. Product Name: 2,4-dimethoxyphenyl benzoate
    2. Synonyms: 2,4-dimethoxyphenyl benzoate
    3. CAS NO:18093-01-1
    4. Molecular Formula:
    5. Molecular Weight: 258.274
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 18093-01-1.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: 2,4-dimethoxyphenyl benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4-dimethoxyphenyl benzoate(18093-01-1)
    11. EPA Substance Registry System: 2,4-dimethoxyphenyl benzoate(18093-01-1)
  • 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: 18093-01-1(Hazardous Substances Data)

18093-01-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18093-01-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,9 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 18093-01:
(7*1)+(6*8)+(5*0)+(4*9)+(3*3)+(2*0)+(1*1)=101
101 % 10 = 1
So 18093-01-1 is a valid CAS Registry Number.

18093-01-1Downstream Products

18093-01-1Relevant articles and documents

Mechanically induced solvent-free esterification method at room temperature

Zheng, Lei,Sun, Chen,Xu, Wenhao,Dushkin, Alexandr V.,Polyakov, Nikolay,Su, Weike,Yu, Jingbo

, p. 5080 - 5085 (2021)

Herein, we describe two novel strategies for the synthesis of esters, as achieved under high-speed ball-milling (HSBM) conditions at room temperature. In the presence of I2 and KH2PO2, the reactions afford the desired esterification derivatives in 45% to 91% yields within 20 min of grinding. Meanwhile, using KI and P(OEt)3, esterification products can be obtained in 24% to 85% yields after 60 min of grinding. In addition, the I2/KH2PO2 protocol was successfully extended to the late-stage diversification of natural products showing the robustness of this useful approach. Further application of this method in the synthesis of inositol nicotinate was also discussed. This journal is

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