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35372-34-0

Ethanimidamide, N-(3-methoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 35372-34-0 Structure

  • Basic information

    1. Product Name: Ethanimidamide, N-(3-methoxyphenyl)-
    2. Synonyms:
    3. CAS NO:35372-34-0
    4. Molecular Formula: C9H12N2O
    5. Molecular Weight: 164.207
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 35372-34-0.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: Ethanimidamide, N-(3-methoxyphenyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethanimidamide, N-(3-methoxyphenyl)-(35372-34-0)
    11. EPA Substance Registry System: Ethanimidamide, N-(3-methoxyphenyl)-(35372-34-0)

  • 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: 35372-34-0(Hazardous Substances Data)

35372-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35372-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,7 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 35372-34:
(7*3)+(6*5)+(5*3)+(4*7)+(3*2)+(2*3)+(1*4)=110
110 % 10 = 0
So 35372-34-0 is a valid CAS Registry Number.

35372-34-0Relevant articles and documents

Practical Synthesis of Benzimidazo[1,2- A[quinolines via Rh(III)-Catalyzed C-H Activation Cascade Reaction from Imidamides and Anthranils

Hu, Yao,Wang, Ting,Liu, Yanzhao,Nie, Ruifang,Yang, Ninghong,Wang, Qiantao,Li, Guo-Bo,Wu, Yong

, p. 501 - 504 (2020)

We report a novel and practical one-pot Rh(III)-catalyzed strategy to construct benzimidazo[1,2-a]quinolines from readily available imidamides and anthranils. The cascade reaction proceeds via a C-H amination-cyclization-cyclization process in ionic liquid without any additives and possesses simple operation, moderate-to-high yield, and broad substrate scope features, which will provide the reference for the construction of biologically active fused benzimidazoles.

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