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4,4'-BIS(3-AMINOPHENOXY)DIPHENYL SULFONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30203-11-3

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30203-11-3 Usage

Chemical Properties

beige to brown powder

Check Digit Verification of cas no

The CAS Registry Mumber 30203-11-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,2,0 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 30203-11:
(7*3)+(6*0)+(5*2)+(4*0)+(3*3)+(2*1)+(1*1)=43
43 % 10 = 3
So 30203-11-3 is a valid CAS Registry Number.

30203-11-3 Well-known Company Product Price

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  • CAS number
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  • TCI America

  • (B1681)  Bis[4-(3-aminophenoxy)phenyl] Sulfone  >98.0%(HPLC)(T)

  • 30203-11-3

  • 25g

  • 470.00CNY

  • Detail
  • Alfa Aesar

  • (A17194)  4,4'-Bis(3-aminophenoxy)diphenyl sulfone, 95%   

  • 30203-11-3

  • 50g

  • 366.0CNY

  • Detail
  • Alfa Aesar

  • (A17194)  4,4'-Bis(3-aminophenoxy)diphenyl sulfone, 95%   

  • 30203-11-3

  • 250g

  • 1365.0CNY

  • Detail
  • Alfa Aesar

  • (A17194)  4,4'-Bis(3-aminophenoxy)diphenyl sulfone, 95%   

  • 30203-11-3

  • 1000g

  • 4067.0CNY

  • Detail

30203-11-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[4-[4-(3-aminophenoxy)phenyl]sulfonylphenoxy]aniline

1.2 Other means of identification

Product number -
Other names Bis[4-(3-aMinophenoxy)phenyl] Sulfone

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:30203-11-3 SDS

30203-11-3Downstream Products

30203-11-3Relevant articles and documents

Synthetic method 4,4 ' -bis (3 -aminophenoxy) diphenyl sulfone

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Paragraph 0023; 0025-0026; 0030-0031, (2021/10/30)

The invention discloses a synthetic method of 4,4 '- bis (3 -aminophenoxy) diphenyl sulphone, which comprises 1, 3 -dinitrobenzene and 4,4 -dihydroxydiphenyl sulfone through nucleophilic substitution reaction in the presence of an alkaline catalyst to generate 4,4' - bis (3 - 3 - '-nitrophenoxy) diphenyl sulfone through catalytic hydrogenation reaction to form bis 3 - (and 4,4-aminophenoxy) diphenyl sulphone. 4,4' . The raw material 1,3 - dinitrobenzene adopted by the synthetic method is only one third of the price of the meta-aminophenol, so that the production cost is greatly reduced. In addition, the reaction temperature is 110 - 120 °C, and compared with the prior art, the reaction temperature is mild and the energy consumption is lower. The synthesis method disclosed by the invention not only is high in reaction yield, but also can obtain higher product purity by adopting n-heptane for recrystallization, the product color is white, the content of metal ions is low, and the synthesis method is suitable for industrial production.

Bis(3-aminophenoxy) aromatics and method of preparing the same

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, (2008/06/13)

Bis(3-nitrophenoxy) derivatives of aromatic or bridged aromatic hydrocarbons are derived from m-dinitrobenzene and dihydroxy derivatives of said hydrocarbons and certain substituted derivatives thereof by a condensation reaction in dipolar aprotic solvents in the presence of bases. The bis(3-nitrophenoxy) derivatives and derivatives obtained are successively reduced to afford bis-(3-aminophenoxy)derivatives. This is a new method for reacting the dihydroxy-derivatives with m-dinitrobenzene, and hence can prepare novel bis(3-aminophenoxy) derivatives such as 4,4'-bis(3-amino-phenoxy)biphenyl, 1-[4-(3-aminophenoxy)phenyl]-1,3,3-trimethyl-6-(3-aminophenoxy)indan, 6,6'-bis(3-aminophenoxy)3,3,3',3'-tetramethyl-1,1'spirobiindan, and methyl substituted 2,2'-bis[4-(3-aminophenoxy)phenyl]propane.

Synthesis of phthalonitrile resins containing ether and imide linkages

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, (2008/06/13)

Imide-containing phthalonitrile monomers are prepared from a phthalonitrile and an aromatic dianhydride. The monomer and a method for preparing the monomer is disclosed. These monomers are synthesized into heat resistant polymers and copolymers with aromatic ring structure incorporating imide and ether linkages. The synthesis of the high temperature thermosetting polymers and copolymers is also disclosed.

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