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ethyl 2-<2'-<1''-(3,4-dimethoxyphenyl)-2''-oxoethyl>-4',5'-dimethoxyphenyl>acetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 40940-49-6 Structure
  • Basic information

    1. Product Name: ethyl 2-<2'-<1''-(3,4-dimethoxyphenyl)-2''-oxoethyl>-4',5'-dimethoxyphenyl>acetic acid
    2. Synonyms: ethyl 2-<2'-<1''-(3,4-dimethoxyphenyl)-2''-oxoethyl>-4',5'-dimethoxyphenyl>acetic acid
    3. CAS NO:40940-49-6
    4. Molecular Formula:
    5. Molecular Weight: 402.444
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 40940-49-6.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: ethyl 2-<2'-<1''-(3,4-dimethoxyphenyl)-2''-oxoethyl>-4',5'-dimethoxyphenyl>acetic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2-<2'-<1''-(3,4-dimethoxyphenyl)-2''-oxoethyl>-4',5'-dimethoxyphenyl>acetic acid(40940-49-6)
    11. EPA Substance Registry System: ethyl 2-<2'-<1''-(3,4-dimethoxyphenyl)-2''-oxoethyl>-4',5'-dimethoxyphenyl>acetic acid(40940-49-6)
  • 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: 40940-49-6(Hazardous Substances Data)

40940-49-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40940-49-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,9,4 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 40940-49:
(7*4)+(6*0)+(5*9)+(4*4)+(3*0)+(2*4)+(1*9)=106
106 % 10 = 6
So 40940-49-6 is a valid CAS Registry Number.

40940-49-6Relevant articles and documents

Synthesis of 3-oxo-2,3-dihydroisoquinolines from ethyl 2-acylphenylacetates and formamides

Venkov,Ivanov

, p. 1145 - 1150 (2007/10/02)

1- and 1,3-substituted 3-oxo-2,3-dihydroisoquinolines 4 are obtained from ethyl 2-acylphenylacetates 3 and formamides.

BENZOPHENANTHRIDINES. I. SYNTHESIS OF 7,12-DIACETOXY-2,3,9,10-TETRAMETHOXY-5,6-DIMETHYLBENZOPHENANTHRIDINIUM PERCHLORATE

Khokhlov, V. A.,Sladkov, V. I.,Kurkovskaya, L. N.,Kuleshova, E. F.,Suvorov, N. N.

, p. 538 - 543 (2007/10/02)

The synthesis of a structural isomer of the highly active antileukemia benzophenathridine alkaloids, i.e., 7,12-diacetoxy-2,3,9,10-tetramethoxy-5,6-dimethylbenzophenanthridinium perchlorate, was realized from 2-hydroxy-3-(3,4-dimethoxyphenyl)-6,7-di

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