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282110-99-0

ethyl 2-(3-methylamino-5-phenyl-2-thenoyl)phenyloxoacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 282110-99-0 Structure

  • Basic information

    1. Product Name: ethyl 2-(3-methylamino-5-phenyl-2-thenoyl)phenyloxoacetate
    2. Synonyms: ethyl 2-(3-methylamino-5-phenyl-2-thenoyl)phenyloxoacetate
    3. CAS NO:282110-99-0
    4. Molecular Formula:
    5. Molecular Weight: 393.463
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 282110-99-0.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 2-(3-methylamino-5-phenyl-2-thenoyl)phenyloxoacetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2-(3-methylamino-5-phenyl-2-thenoyl)phenyloxoacetate(282110-99-0)
    11. EPA Substance Registry System: ethyl 2-(3-methylamino-5-phenyl-2-thenoyl)phenyloxoacetate(282110-99-0)

  • 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: 282110-99-0(Hazardous Substances Data)

282110-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 282110-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,2,1,1 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 282110-99:
(8*2)+(7*8)+(6*2)+(5*1)+(4*1)+(3*0)+(2*9)+(1*9)=120
120 % 10 = 0
So 282110-99-0 is a valid CAS Registry Number.

282110-99-0Downstream Products

282110-99-0Relevant articles and documents

A facile and convenient synthesis of 3-alkylamino-5-arylthiophenes with a variety of substituents at C-2 and studies of reaction mechanisms

Kim, Bo Sung,Kim, Kyongtae

, p. 3690 - 3699 (2007/10/03)

Thioaroylketene S,N-acetals were treated with active methylene compounds including β-keto ester, nitromethane, cyanoacetic acid, p- toluenesulfonylacetone, 4-nitrophenylacetic acid, and diethyl (2- oxopropyl)phosphonate in the presence of mercury(II) acetate in CH2Cl2 at room temperature. These reactions gave 3-alkylamino-5-arylthiophenes containing various substituents, which comprised, respectively, alkoxycarbonyl, nitro, cyano, p-toluenesulfonyl, 4-nitrophenyl, and diethylphosphono groups at C-2 in good yields. The reaction of 3-methylamino- 3-methylthio-1-phenylthioxopropene with malonic acid or Meldrum's acid under the same conditions gave 3-methylamino-5-phenylthiophene. Similarly, treatment of 3-methylamino-3-methylthio-1-phenylthioxopropene with various enolizable cyclic ketones such as 4-hydroxy-6-methyl-2-pyrone, homophthalic anhydride, 2-hydroxy1,4-benzoquinone, and 1,3-diethyl-2-thiobarbituric acid gave thieno[3,2-b]pyridin-4-one, thieno[3,2c]isoquinolin-5-one, thieno[3,2- c]benzazepine-1,6-dione, and thieno[3,2-d]pyrimidine-2,4-dione, respectively.

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