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CAS

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26253-37-2

Benzenamine, N,N-bis(2-phenoxyethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 26253-37-2 Structure

  • Basic information

    1. Product Name: Benzenamine, N,N-bis(2-phenoxyethyl)-
    2. Synonyms:
    3. CAS NO:26253-37-2
    4. Molecular Formula: C22H23NO2
    5. Molecular Weight: 333.43
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 26253-37-2.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: Benzenamine, N,N-bis(2-phenoxyethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenamine, N,N-bis(2-phenoxyethyl)-(26253-37-2)
    11. EPA Substance Registry System: Benzenamine, N,N-bis(2-phenoxyethyl)-(26253-37-2)

  • 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: 26253-37-2(Hazardous Substances Data)

26253-37-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26253-37-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,2,5 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 26253-37:
(7*2)+(6*6)+(5*2)+(4*5)+(3*3)+(2*3)+(1*7)=102
102 % 10 = 2
So 26253-37-2 is a valid CAS Registry Number.

26253-37-2Downstream Products

26253-37-2Relevant articles and documents

A simple method for N-phenoxyethylation of anilines

Romanelli,Jios,Guaymas,Piovoso,Autino

, p. 562 - 563 (2000)

We wanted to search for new reaction conditions to prepare the title compounds, to be checked later in novel syntheses of heterocyclic compounds. To the best of our knowledge, there was no report in the literature of any well-established method for the pr

Catalytic N-Alkylation of Amines Using Carboxylic Acids and Molecular Hydrogen

Sorribes, Iván,Cabrero-Antonino, Jose R.,Vicent, Cristian,Junge, Kathrin,Beller, Matthias

, p. 13580 - 13587 (2015/11/10)

A convenient, practical and green N-alkylation of amines has been accomplished by applying readily available carboxylic acids in the presence of molecular hydrogen. Applying an in situ formed ruthenium/triphos complex and an organic acid as cocatalyst, a broad range of alkylated secondary and tertiary amines are obtained in good to excellent yields. This novel method is also successfully applied for the synthesis of unsymmetrically substituted N-methyl/alkyl anilines through a direct three-component coupling reaction of the corresponding amines, carboxylic acids, and CO2 as a C1 source.

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