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2-benzenesulfonyl-1,4-dichlorobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38346-45-1

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38346-45-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38346-45-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,3,4 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 38346-45:
(7*3)+(6*8)+(5*3)+(4*4)+(3*6)+(2*4)+(1*5)=131
131 % 10 = 1
So 38346-45-1 is a valid CAS Registry Number.

38346-45-1Downstream Products

38346-45-1Relevant academic research and scientific papers

POLYARYLENE POLYMERS AND PROCESSES FOR PREPARING

-

, (2012/01/14)

Provided are sulfone-containing polyarylene polymers. Also provided are monomers and processes for preparing the polymers. The polyarylene polymers are suitable for use as engineering polymers.

Advances in Ni(0)-catalyzed coupling for the synthesis of polythiophenes and polyphenylenes

Hagberg, Erik C.,Olson, David A.,Sheares, Valerie V.

, p. 4748 - 4754 (2007/10/03)

The effects of solvent and monomer structure on the Ni(0)-catalyzed polymerization of 2,5-dichloro-3-(2′-thiophenecarbonyl)thiophene, 3-benzenesulfonyl-2,5-dichlorothiophene, 2,5-dichlorobenzophenone, and 2-benzenesulfonyl-1,4-dichlorobenzene were explored. Poly[3-(2′- thiophenecarbonyl)-2,5-thiophene] with an intrinsic viscosity of 0.38 dL/g and a 10% weight loss temperature in nitrogen of 480 °C (Tg = 149 °C) was synthesized. Oligomeric material was prepared from 3-benzenesulfonyl-2,5-dichlorothiophene. Poly(2,5-benzophenone) of 58 × 103 g/mol ([η] = 1.15 dL/g) with a Tg of 180 °C and a 10% weight loss temperature in nitrogen of 576 °C was synthesized. Oligomeric materials were also obtained from the polymerization of 2-benzenesulfonyl-1,4-dichlorobenzene. It was shown that the solvent choice has drastic effects upon the catalyst system and the final polymer. The differences in the catalyst resulting from solvent choice were explored by nuclear magnetic resonance. Effects arising from the structure of the monomer are discussed in relationship to the results obtained and the proposed mechanism.

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