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144294-13-3

Imidazo[1,2-a]pyrazine-3-carboxylic acid, 2-phenyl-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 144294-13-3 Structure

  • Basic information

    1. Product Name: Imidazo[1,2-a]pyrazine-3-carboxylic acid, 2-phenyl-, ethyl ester
    2. Synonyms:
    3. CAS NO:144294-13-3
    4. Molecular Formula: C15H13N3O2
    5. Molecular Weight: 267.287
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144294-13-3.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: Imidazo[1,2-a]pyrazine-3-carboxylic acid, 2-phenyl-, ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Imidazo[1,2-a]pyrazine-3-carboxylic acid, 2-phenyl-, ethyl ester(144294-13-3)
    11. EPA Substance Registry System: Imidazo[1,2-a]pyrazine-3-carboxylic acid, 2-phenyl-, ethyl ester(144294-13-3)

  • 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: 144294-13-3(Hazardous Substances Data)

144294-13-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144294-13-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,2,9 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 144294-13:
(8*1)+(7*4)+(6*4)+(5*2)+(4*9)+(3*4)+(2*1)+(1*3)=123
123 % 10 = 3
So 144294-13-3 is a valid CAS Registry Number.

144294-13-3Relevant articles and documents

Synthesis of imidazopyridines via copper-catalyzed, formal aza-[3 + 2] cycloaddition reaction of pyridine derivatives with α-diazo oxime ethers

Park, Sangjune,Kim, Hyunseok,Son, Jeong-Yu,Um, Kyusik,Lee, Sooho,Baek, Yonghyeon,Seo, Boram,Lee, Phil Ho

, p. 10209 - 10218 (2017)

The Cu-catalyzed, formal aza-[3 + 2] cycloaddition reaction of pyridine derivatives with α-diazo oxime ethers in trifluoroethanol was used to synthesize imidazopyridines via the release of molecular nitrogen and elimination of alcohol. These methods enabled modular synthesis of a wide range of N-heterobicyclic compounds such as imidazopyridazines, imidazopyrimidines, and imidazopyrazines with an α-imino Cu-carbenoid generated from the α-diazo oxime ethers and copper.

Research on heterocyclic compounds, XXIX. Synthesis and antiinflammatory activity of imidazo[1,2-a]pyrazine derivatives

Abignente,De Caprariis,Rimoli,Capasso,Autore

, p. 919 - 930 (2007/10/02)

The reaction in anhydrous ethanol of some substituted 2-aminopyrazines with ethyl 2-benzoyl-2-bromoacetate or with ethyl 3-bromo-4-oxopentanoate afforded a group of ethyl 2-phenylimidazo[1,2-a]pyrazine-3-carboxylates and a group of ethyl 2-methylimidazo[1

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