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28059-59-8

N,N-dimethyl-2-benzylaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 28059-59-8 Structure

  • Basic information

    1. Product Name: N,N-dimethyl-2-benzylaniline
    2. Synonyms: N,N-dimethyl-2-benzylaniline
    3. CAS NO:28059-59-8
    4. Molecular Formula:
    5. Molecular Weight: 211.307
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 28059-59-8.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: N,N-dimethyl-2-benzylaniline(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N-dimethyl-2-benzylaniline(28059-59-8)
    11. EPA Substance Registry System: N,N-dimethyl-2-benzylaniline(28059-59-8)

  • 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: 28059-59-8(Hazardous Substances Data)

28059-59-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28059-59-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,0,5 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 28059-59:
(7*2)+(6*8)+(5*0)+(4*5)+(3*9)+(2*5)+(1*9)=128
128 % 10 = 8
So 28059-59-8 is a valid CAS Registry Number.

28059-59-8Relevant articles and documents

Thermal rearrangement of N-benzylanilinium hexafluoroantimonates

Park, Jeongkyu,Shin, Jung-Hyu,Lee, Changjin

, p. 7485 - 7488 (1999)

We prepared p-substituted N-benzylanilinium hexafluoroantimonates, known cationic initiators, and examined their thermal reaction. The thermal reaction produced 2- or 4-benzylanilinium salts as the major products, which resulted from the rearrangement of the benzyl group. The reaction proceeded at lower temperature with higher yield when the substituent in the benzyl group was electron donating.

Thermal reactions of N-Alkyl-2-benzylaniline and N-Alkyl-N′-phenyl-o- phenylenediamine: An unusual route to 2-phenylindole and 2-phenylbenzimidazole

Creencia, Evelyn Cuevas,Taguchi, Kei,Horaguchi, Takaaki

, p. 837 - 843 (2008/09/21)

(Chemical Equation Presented) Thermal cyclization reactions of N-alkyl-2-benzylaniline 1a-d and N-alkyl-N′-phenyl-o-phenylenediamine 2a-b were carried out expecting to get seven-membered heterocyclic compounds. However, the results show that aside from th

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