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2,3-Difluoro-4-(phenyldiazenyl)phenol is a chemical compound with the molecular formula C12H8F2N2O. It is a diazo compound, characterized by the presence of an azo group (-N=N-) attached to a phenyl ring. 2,3-DIFLUORO-4-(PHENYLDIAZENYL)PHENOL also features two fluorine atoms at the 2 and 3 positions on the phenyl ring, contributing to its unique properties. Known for its bright and colorful appearance, it is commonly utilized in the creation of dyes and pigments for various applications.

847872-04-2

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847872-04-2 Usage

Uses

Used in Inks and Paints:
2,3-Difluoro-4-(phenyldiazenyl)phenol is used as a dye or pigment in the ink and paint industry for its vibrant color and stability. Its bright and colorful appearance enhances the visual appeal of these products, making them suitable for a wide range of applications, from artistic endeavors to industrial coatings.
Used in Plastics:
In the plastics industry, 2,3-difluoro-4-(phenyldiazenyl)phenol is employed as a colorant to impart specific hues to plastic materials. Its compatibility with various polymers and resistance to fading under different conditions make it an ideal choice for creating aesthetically pleasing and durable plastic products.
Used in Research and Development:
2,3-Difluoro-4-(phenyldiazenyl)phenol is also used in research and development settings for its potential biological and pharmaceutical applications. Scientists are investigating its properties to explore possible uses in medicine, although further studies are required to fully understand its capabilities and safety in these areas.

Check Digit Verification of cas no

The CAS Registry Mumber 847872-04-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,8,7 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 847872-04:
(8*8)+(7*4)+(6*7)+(5*8)+(4*7)+(3*2)+(2*0)+(1*4)=212
212 % 10 = 2
So 847872-04-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H8F2N2O/c13-11-9(6-7-10(17)12(11)14)16-15-8-4-2-1-3-5-8/h1-7,17H/b16-15+

847872-04-2 Well-known Company Product Price

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  • Alfa Aesar

  • (H32573)  2,3-Difluoro-4-hydroxyazobenzene, 98+%   

  • 847872-04-2

  • 250mg

  • 365.0CNY

  • Detail
  • Alfa Aesar

  • (H32573)  2,3-Difluoro-4-hydroxyazobenzene, 98+%   

  • 847872-04-2

  • 1g

  • 1005.0CNY

  • Detail
  • Alfa Aesar

  • (H32573)  2,3-Difluoro-4-hydroxyazobenzene, 98+%   

  • 847872-04-2

  • 5g

  • 3357.0CNY

  • Detail

847872-04-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-difluoro-4-(phenylhydrazinylidene)cyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names 2,3-DIFLUORO-4-(PHENYLDIAZENYL)PHENOL

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:847872-04-2 SDS

847872-04-2Downstream Products

847872-04-2Relevant academic research and scientific papers

Process for the preparation of halogen containing 4-amino phenols

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Page/Page column 8; 9, (2010/02/11)

Production of 4-aminophenol derivatives (I) comprises converting an aniline (II) to a diazonium salt (III), reacting (III) with a phenol (IV) in the presence of a base to give a phenylazophenol (V), and reacting (V) with a reducing agent and optionally O-alkylating the product. Production of 4-aminophenol derivatives of formula (I) comprises converting an aniline of formula (II) to a diazonium salt of formula (III), reacting (III) with a phenol of formula (IV) in the presence of a base to give a phenylazophenol of formula (V), and reacting (V) with a reducing agent and optionally O-alkylating the product: [Image] m : 0-3; n : 1-4; m+n : 4 or less; R 1>H, 1-12C alkyl or 5-15C aralkyl; R 2>1-12C fluoroalkyl, 1-12C fluoroalkylthio or 1-12C fluoroalkoxy; Hal : Br, Cl or F; R 3>halo, CN, SCN, SO 3M, NO 2, 1-12C alkyl, 1-12C fluoroalkyl, 1-12C fluoroalkylthio,1-12C fluoroalkoxy, 1-12C alkoxy, 1-12C alkoxycarbonyl, di(1-12C alkyl)amino, 4-14C aryl or 5-15C aralkyl; M : H or alkali metal; p : 0-3; An : an anion. Independent claims are also included for: (1) compounds (I) other than 4-amino-3,5-difluorophenol, 4-amino-2,5-difluorophenol, 4-amino-2,6-difluorophenol, 4-amino-2-chloro-6-fluorophenol, 4-amino-2-chloro-3-fluorophenol, 4-amino-2-chloro-5-fluorophenol, 4-amino-2-bromo-5-fluorophenol, 4-amino-2-fluorophenol, 4-amino-3-fluorophenol, 4-amino-5-chloro-2-(trifluoromethyl)phenol, 4-amino-2-chloro-6-(trifluoromethyl)phenol and (it is stated) 4-amino-2-(trifluoromethyl)phenol and 4-amino-3-(trifluoromethyl)phenol; compounds (V) other than 3,5-difluoro-4-phenylazo-phenol, 3-fluoro-4-phenylazophenol, 3-fluoro-4-(4'-nitrophenylazo)-phenol, 3-fluoro-4-(3'-nitrophenylazo)-phenol, 3-fluoro-4-(4'-thiocyanatophenylazo)-phenol, 3-fluoro-4-(4'-sulfophenylazo)-phenol, 4-(2'-fluoro-4'-hydroxyphenylazo)benzoic acid ethyl ester, 2-fluoro-4-(4'-fluorophenylazo)-phenol, 2-fluoro-4-(3'-fluorophenylazo)-phenol, 2-fluoro-4-(4'-sulfophenylazo)-phenol, 4-(3'-fluoro-4'-hydroxyphenylazo)benzoic acid ethyl ester, 2,3-difluoro-4-(4'-iodphenylazo)-phenol; 2,3-difluoro-4-(4'sulfophenylazo)-phenol, 2,6-difluoro-4-(2'-bromphenylazo)-phenol and (it is stated) 3-(trifluoromethyl)-4-(phenylazo)-phenol and 3-(trifluoromethyl)-4-(4'-sodiumsulfonatophenylazo)-phenol.

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