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2-(N-o-methoxalylphenylaminomethylene)-3(2H)-benzothiophenone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

126045-12-3

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  • 126045-12-3 Structure

  • Basic information

    1. Product Name: 2-(N-o-methoxalylphenylaminomethylene)-3(2H)-benzothiophenone
    2. Synonyms:
    3. CAS NO:126045-12-3
    4. Molecular Formula:
    5. Molecular Weight: 339.372
    6. EINECS: N/A
    7. Product Categories: N/A

  • 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-(N-o-methoxalylphenylaminomethylene)-3(2H)-benzothiophenone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(N-o-methoxalylphenylaminomethylene)-3(2H)-benzothiophenone(126045-12-3)
    11. EPA Substance Registry System: 2-(N-o-methoxalylphenylaminomethylene)-3(2H)-benzothiophenone(126045-12-3)

  • 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: 126045-12-3(Hazardous Substances Data)

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126045-12-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126045-12-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,0,4 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 126045-12:
(8*1)+(7*2)+(6*6)+(5*0)+(4*4)+(3*5)+(2*1)+(1*2)=93
93 % 10 = 3
So 126045-12-3 is a valid CAS Registry Number.

126045-12-3Downstream Products

126045-12-3Relevant academic research and scientific papers

BENZOID-QUINOID TAUTOMERISM IN AZOMETHINES AND THEIR STRUCTURAL ANALOGS. 46. SYNTHESIS AND REACTIONS OF 2-(N-ISATINOMETHYLENE)-3(2H)-BENZOTHIOPHENONE

Bren', Zh. V.,Rybalkin, V. P.,Bren', V. A.

, p. 1018 - 1021 (2007/10/02)

Electronic, IR and UV spectroscopy has shown that 2-(N-isatinomethylene)-3(2H)-benzothiophenone in solution displays photo- and solvatochromism as a result of reversible E -> Z isomerization, and it readily undergoes alcoholysis of the lactam bond.The resulting aminovinyl ketones exist as mixtures of the thermodynamically stable E- and Z-isomers.

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