Welcome to LookChem.com Sign In|Join Free
  • or
1,3,5-Triazin-2-amine, 4,6-dichloro-N-[4-[(4-nitrophenyl)azo]phenyl]- is a complex organic compound with the chemical formula C13H8Cl2N6O2. It is a derivative of 1,3,5-triazine, a heterocyclic compound consisting of three nitrogen atoms and three carbon atoms. The molecule features two chlorine atoms at the 4 and 6 positions, an amino group at the 2 position, and a complex azo group attached to the nitrogen at the 1 position. The azo group consists of a 4-nitrophenyl group connected to a phenyl group through an azo bond. 1,3,5-Triazin-2-amine, 4,6-dichloro-N-[4-[(4-nitrophenyl)azo]phenyl]- is known for its potential applications in the synthesis of dyes and pigments, as well as its use in various chemical research and industrial processes. Due to its complex structure and functional groups, it exhibits unique chemical properties and reactivity, making it an interesting subject for study in the field of organic chemistry.

5664-79-9

Post Buying Request

5664-79-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

5664-79-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5664-79-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,6 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5664-79:
(6*5)+(5*6)+(4*6)+(3*4)+(2*7)+(1*9)=119
119 % 10 = 9
So 5664-79-9 is a valid CAS Registry Number.

5664-79-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-dichloro-N-[4-[(4-nitrophenyl)diazenyl]phenyl]-1,3,5-triazin-2-amine

1.2 Other means of identification

Product number -
Other names -

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:5664-79-9 SDS

5664-79-9Downstream Products

5664-79-9Relevant academic research and scientific papers

Dye compound as well as preparation method and application thereof

-

Paragraph 0038; 0040-0043; 0055-0060; 0072-0077, (2019/07/01)

The invention discloses a dye compound. The structural formula of the compound is shown as a formula (I). The invention particularly relates to a dye compound as well as a preparation method and application thereof, and belongs to the technical field of t

Cation active dye containing azo structure and preparing method of cation active dye

-

Paragraph 0106; 0107; 0114; 0115, (2017/12/09)

The invention provides a cation active dye containing an azo structure and a preparing method of the cation active dye. The cation active dye is shown in the description. The preparing method comprises the steps of firstly using a secondary amine compound to react with methoxypoly (ethylene glycol) glycidyl ether to prepare a 2-hydroxy-3-methyl polyether-base substituted propyl tertiary amine compound, then using halo-triazine to connect azo-disperse dye color body containing hydroxyl groups or amino groups, and finally conducting quaternization on tertiary amine in the product to prepare the cation active dye containing the azo structure. The cation active dye has a complete color spectrum, the water solubility is adjustable, the cellulosic fiber is high in substantivity, saltless dyeing can be conducted, the preparing method is simple and the cost is low.

Nucleophilic Substitutions in 1,3,5-Triazines. VII. The Kinetic and Mechanism of Cyanuric Chloride with 4'-Substituted 4-Aminoazobenzens

Havlik, I.,Bacaloglu, R.

, p. 936 - 942 (2007/10/02)

The kinetic and mechanism of cyanuric chloride reaction with 4'-substituted 4-aminoazobenzens in dioxan-water was studied by conductometry.An addition-elimination mechanism with a monomolecular elimination of chlorine ion at low water concentrations or a

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 5664-79-9