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102101-10-0

ethyl (E)-2-cyano-3-(3-methylphenylamino)-3-(methylthio)acrylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 102101-10-0 Structure

  • Basic information

    1. Product Name: ethyl (E)-2-cyano-3-(3-methylphenylamino)-3-(methylthio)acrylate
    2. Synonyms: ethyl (E)-2-cyano-3-(3-methylphenylamino)-3-(methylthio)acrylate
    3. CAS NO:102101-10-0
    4. Molecular Formula:
    5. Molecular Weight: 276.359
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 102101-10-0.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 (E)-2-cyano-3-(3-methylphenylamino)-3-(methylthio)acrylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl (E)-2-cyano-3-(3-methylphenylamino)-3-(methylthio)acrylate(102101-10-0)
    11. EPA Substance Registry System: ethyl (E)-2-cyano-3-(3-methylphenylamino)-3-(methylthio)acrylate(102101-10-0)

  • 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: 102101-10-0(Hazardous Substances Data)

102101-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102101-10-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,1,0 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 102101-10:
(8*1)+(7*0)+(6*2)+(5*1)+(4*0)+(3*1)+(2*1)+(1*0)=30
30 % 10 = 0
So 102101-10-0 is a valid CAS Registry Number.

102101-10-0Downstream Products

102101-10-0Relevant articles and documents

Highly selective and efficient synthesis of 3-arylamino-substituted 5-aminopyrazole-4-carboxylates under microwave irradiation

Lim, Felicia Phei Lin,Gan, Rowena Xin Yi,Dolzhenko, Anton V.

, p. 775 - 778 (2017)

An improved microwave-assisted method was developed for the preparation of ethyl 5-aminopyrazole carboxylates from ethyl 2-cyano-3-methylthioacrylates and hydrazine. It was shown that using microwave irradiation significantly reduced the reaction time and improved the process selectivity and yield. The reaction proved to be reproducible in different microwave reactors and on large scale, affording the desired products in high yields and purity. A representative library of 3-arylamino-substituted 5-aminopyrazole-4-carboxylates was successfully prepared to assess the scope of the method.

1H and 13C NMR spectral characterization of some antimalarial in vitro 2,4-diamino-10-methylpyrimido[4,5-b]-5-quinolone derivatives

Charris, Jaime E.,Dominguez, Jose N.,Gamboa, Neira,Angel, Jorge,Pina, Nolberto,Guerra, Mayamaru,Michelena, Elba,Lopez, Simon E.

, p. 477 - 479 (2007/10/03)

We report the 1H NMR and 13C NMR chemical shifts and J(H,H), J(H,F) and J(C,F) coupling constants of 13 2,4-diamino-10-methylpyrimido[4,5-b]-5-quinolone derivatives, some of them with moderate activity against Plasmodium falciparum i

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