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CAS

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331838-04-1

N-(2,4-difluorophenyl)-4-nitrobenzenecarboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 331838-04-1 Structure

  • Basic information

    1. Product Name: N-(2,4-difluorophenyl)-4-nitrobenzenecarboxamide
    2. Synonyms: N-(2,4-difluorophenyl)-4-nitrobenzenecarboxamide
    3. CAS NO:331838-04-1
    4. Molecular Formula: C13H8F2N2O3
    5. Molecular Weight: 278.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 331838-04-1.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-(2,4-difluorophenyl)-4-nitrobenzenecarboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2,4-difluorophenyl)-4-nitrobenzenecarboxamide(331838-04-1)
    11. EPA Substance Registry System: N-(2,4-difluorophenyl)-4-nitrobenzenecarboxamide(331838-04-1)

  • 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: 331838-04-1(Hazardous Substances Data)

331838-04-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 331838-04-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,1,8,3 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 331838-04:
(8*3)+(7*3)+(6*1)+(5*8)+(4*3)+(3*8)+(2*0)+(1*4)=131
131 % 10 = 1
So 331838-04-1 is a valid CAS Registry Number.

331838-04-1Downstream Products

331838-04-1Relevant articles and documents

Preparation of amides mediated by isopropylmagnesium chloride under continuous flow conditions

Munoz, Juan De M.,Alcazar, Jesus,De La Hoz, Antonio,Diaz-Ortiz, Angel,Alonso De Diego, Sergio-A.

supporting information; experimental part, p. 1335 - 1341 (2012/06/04)

A safe, green and functional-group-tolerant flow version of the direct amide bond formation mediated by Grignard reagents (the Bodroux reaction) is described. The procedure can be applied to a wide variety of primary and secondary amines and anilines, as well as to aromatic and aliphatic esters. The flow approach leads to improved yields and selectivities in the reaction, which has a sustainable purification procedure and a simple scale-up. This reaction represents an efficient and green alternative to the use of alkylaluminium and metal-catalyzed procedures.

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