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124411-43-4

N-(2-methoxyphenyl)-3-methylbenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124411-43-4 Structure

  • Basic information

    1. Product Name: N-(2-methoxyphenyl)-3-methylbenzamide
    2. Synonyms: N-(2-methoxyphenyl)-3-methylbenzamide
    3. CAS NO:124411-43-4
    4. Molecular Formula: C15H15NO2
    5. Molecular Weight: 241.2851
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124411-43-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-(2-methoxyphenyl)-3-methylbenzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2-methoxyphenyl)-3-methylbenzamide(124411-43-4)
    11. EPA Substance Registry System: N-(2-methoxyphenyl)-3-methylbenzamide(124411-43-4)

  • 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: 124411-43-4(Hazardous Substances Data)

124411-43-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124411-43-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,1 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 124411-43:
(8*1)+(7*2)+(6*4)+(5*4)+(4*1)+(3*1)+(2*4)+(1*3)=84
84 % 10 = 4
So 124411-43-4 is a valid CAS Registry Number.

124411-43-4Downstream Products

124411-43-4Relevant articles and documents

An efficient, one-pot transamidation of 8-aminoquinoline amides activated by tertiary-butyloxycarbonyl

Wu, Wengang,Yi, Jun,Xu, Huipeng,Li, Shuangjun,Yuan, Rongxin

, (2019/04/05)

The efficient, one-pot access to the transamidation of 8-aminoquinoline (8-AQ), notorious for its harsh removal conditions, has been widely employed as an auxiliary in C–H functionalization reactions due to its strong directing ability. In this study, the facile and mild Boc protection of the corresponding 8-AQ amide was critical to activate the amide C(acyl)–N bond by twisting its geometry to lower the amidic resonance energy. Both aryl and alkyl amines proceeded transamidation in one-pot, user-friendly conditions with excellent yields.

Amide Boc de-protection method

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Paragraph 0035; 0109; 0110; 0111, (2018/09/13)

The invention discloses an amide Boc de-protection method. The amide Boc de-protection method includes carrying out reaction on Boc protected amide III and amine IV under the condition of the presenceof palladium catalysts to generate new amide V. 8-aminoquinoline can be used as a guide group to be applied to chemical reaction, a process for synthesizing the new amide by means of de-protection isprovided, protecting groups can be easily removed by means of palladium catalysis, the new amide can be generated, and the reaction is high in efficiency. The amide Boc de-protection method has the advantages of environmental friendliness, recyclability and the like.

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