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1345509-63-8

ethyl 1,2,4-triphenyl-1H-imidazole-5-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1345509-63-8 Structure

  • Basic information

    1. Product Name: ethyl 1,2,4-triphenyl-1H-imidazole-5-carboxylate
    2. Synonyms: ethyl 1,2,4-triphenyl-1H-imidazole-5-carboxylate
    3. CAS NO:1345509-63-8
    4. Molecular Formula:
    5. Molecular Weight: 368.435
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1345509-63-8.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 1,2,4-triphenyl-1H-imidazole-5-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 1,2,4-triphenyl-1H-imidazole-5-carboxylate(1345509-63-8)
    11. EPA Substance Registry System: ethyl 1,2,4-triphenyl-1H-imidazole-5-carboxylate(1345509-63-8)

  • 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: 1345509-63-8(Hazardous Substances Data)

1345509-63-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1345509-63-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,5,5,0 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1345509-63:
(9*1)+(8*3)+(7*4)+(6*5)+(5*5)+(4*0)+(3*9)+(2*6)+(1*3)=158
158 % 10 = 8
So 1345509-63-8 is a valid CAS Registry Number.

1345509-63-8Downstream Products

1345509-63-8Relevant articles and documents

Facile Synthesis of Polysubstituted Imidazoles through CBr4-Mediated Tandem Cyclization of Amidines with 1,3-Dicarbonyl Compounds or Ketones

Zhou, Xiaoqiang,Ma, Haojie,Shi, Chong,Zhang, Yixin,Liu, XingXing,Huang, Guosheng

, p. 237 - 240 (2017)

Polysubstituted imidazoles were synthesized in a facile metal-free CBr4-mediated tandem cyclization of amidine with 1,3-dicarbonyl compounds or ketones. The desired products were obtained in moderate to good yields by using simple operation tec

A practical metal-free route to 1,2,4,5-tetrasubstituted imidazoles derivatives from the annulation of amidines and β-keto esters

Zhang, Xueguo,Wu, Ping,Fu, Yajie,Zhang, Fangdong,Chen, Baohua

supporting information, p. 870 - 873 (2017/02/18)

A new practical carbon-nitrogen bond formation reaction of amidines with ethyl acetoacetate to synthesize imidazoles via oxidative cyclization in the presence of bromide. The reactions were occured under mild and metal-free conditions.

Catalyst-free preparation of 1,2,4,5-tetrasubstituted imidazoles from a novel unexpected domino reaction of 2-azido acrylates and nitrones

Hu, Bao,Wang, Zhao,Ai, Ning,Zheng, Jie,Liu, Xing-Hai,Shan, Shang,Wang, Zhongwen

experimental part, p. 6362 - 6365 (2012/01/14)

A highly efficient and convenient method for the synthesis of 1,2,4,5-tetrasubstituted imidazoles from readily accessible 2-azido acrylates and nitrones has been developed. This reaction proceeded under mild conditions without the assistance of any metal,

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