Welcome to LookChem.com Sign In|Join Free

CAS

  • or

6364-03-0

N-Ethyl-N-phenyl-2-naphthylamine is an organic compound with the chemical formula C20H17N. It is a derivative of 2-naphthylamine, where one hydrogen atom is replaced by an ethyl group and another by a phenyl group. This yellow crystalline solid is primarily used as an intermediate in the synthesis of various dyes and pigments, particularly those with a blue or green hue. The compound is also known for its potential applications in the pharmaceutical industry. However, it is important to note that N-Ethyl-N-phenyl-2-naphthylamine is classified as a suspected carcinogen, and therefore, it requires careful handling and proper safety measures during its production and use.

6364-03-0 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 6364-03-0 Structure

  • Basic information

    1. Product Name: N-Ethyl-N-phenyl-2-naphthylamine
    2. Synonyms: N-Ethyl-N-phenyl-2-naphthylamine
    3. CAS NO:6364-03-0
    4. Molecular Formula: C18H17N
    5. Molecular Weight: 247.33428
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 6364-03-0.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-Ethyl-N-phenyl-2-naphthylamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-Ethyl-N-phenyl-2-naphthylamine(6364-03-0)
    11. EPA Substance Registry System: N-Ethyl-N-phenyl-2-naphthylamine(6364-03-0)

  • 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: 6364-03-0(Hazardous Substances Data)

6364-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6364-03-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,6 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6364-03:
(6*6)+(5*3)+(4*6)+(3*4)+(2*0)+(1*3)=90
90 % 10 = 0
So 6364-03-0 is a valid CAS Registry Number.

6364-03-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethyl-N-phenylnaphthalen-2-amine

1.2 Other means of identification

Product number -
Other names Aethyl-[2]naphthyl-phenyl-amin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6364-03-0 SDS

6364-03-0Downstream Products

6364-03-0Relevant articles and documents

Metal-Free Oxidative C-C Coupling of Arylamines Using a Quinone-Based Organic Oxidant

Maddala, Sudhakar,Mallick, Sudesh,Venkatakrishnan, Parthasarathy

, p. 8958 - 8972 (2017/09/11)

A variety of arylamines are shown to undergo oxidative C-C bond formation using quinone-based chloranil/H+ reagent as the recyclable organic (metal-free) oxidant system to afford benzidines/naphthidines. Arylamines (3°/2°) designed with various substituents were employed to understand the steric as well as electronic preferences of oxidative dimerization, and a mechanism involving amine radical cation has been proposed. The tetraphenylbenzidine derivative obtained via oxidative C-C coupling has been further converted to blue-emissive hole-transporting material via a simple chemical transformation. This study highlights the preparation of novel HTMs in a simple, economic, and efficient manner.

A simple route to benz[a]acridinium salts

Hartmann, Horst

experimental part, p. 711 - 714 (2011/09/20)

By reaction of N-substituted N-phenyl-2-naphthylamimes with the Vilsmeier reagent N-substituted benz[a]acridinium salts are formed in satisfactory yields. 2011 Verlag der Zeitschrift fuer Naturforschung, Tuebingen.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 6364-03-0