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6050-13-1

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6050-13-1 Usage

Chemical Properties

Powder

Purification Methods

After removing free acid by extraction with cold aqueous Na2CO3, the residue is crystallised from acetic anhydride and dried at 100o. Acetic anhydride converts the acid to the anhydride. It also crystallises from *C6H6 (m 219o) or chlorobenzene (m 224.5-225.5o). [Beilstein 17 H 526, 17 II 495, 17 III/IV 6425.]

Check Digit Verification of cas no

The CAS Registry Mumber 6050-13-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,5 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6050-13:
(6*6)+(5*0)+(4*5)+(3*0)+(2*1)+(1*3)=61
61 % 10 = 1
So 6050-13-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H8O3/c15-13-11-7-3-1-5-9(11)10-6-2-4-8-12(10)14(16)17-13/h1-8H

6050-13-1 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (B23415)  Diphenic anhydride, 98%   

  • 6050-13-1

  • 10g

  • 430.0CNY

  • Detail
  • Alfa Aesar

  • (B23415)  Diphenic anhydride, 98%   

  • 6050-13-1

  • 50g

  • 1429.0CNY

  • Detail
  • Alfa Aesar

  • (B23415)  Diphenic anhydride, 98%   

  • 6050-13-1

  • 250g

  • 6010.0CNY

  • Detail
  • Aldrich

  • (148903)  Diphenicanhydride  98%

  • 6050-13-1

  • 148903-10G

  • 713.70CNY

  • Detail

6050-13-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Diphenic anhydride

1.2 Other means of identification

Product number -
Other names Dibenz[c,e]oxepin-5,7-dione

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:6050-13-1 SDS

6050-13-1Relevant articles and documents

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Manukian

, p. 1999,2003 (1965)

-

Synthesis and Evaluation of Antibacterial Activity of 1,2,4-Oxadiazole-Containing Biphenylcarboxylic Acids

Baikov, S. V.,Presnukhina, S. I.,Shetnev, A. A.,Tarasenko, M. V.

, p. 1611 - 1619 (2020/10/15)

Abstract: A one-pot method for the synthesis of biphenylcarboxylic acids containing 1,2,4-oxadiazole ring in the NaOH–DMSO system was developed. The results of in vitro experiments showed that the synthesized compounds exhibit antibacterial activity against susceptible strains of E. coli and S. aureus.

Oxidation of Polynuclear Aromatic Hydrocarbons using Ruthenium-Ion-Catalyzed Oxidation: The Role of Aromatic Ring Number in Reaction Kinetics and Product Distribution

Nowicka, Ewa,Clarke, Tomos J.,Sankar, Meenakshisundaram,Jenkins, Robert L.,Knight, David W.,Golunski, Stanislaw,Hutchings, Graham J.,Willock, David J.,Francisco, Manuel,Taylor, Stuart H.

, p. 655 - 662 (2018/01/26)

Oxidation of aromatic hydrocarbons with differing numbers of fused aromatic rings (2–5), have been studied in two solvent environments (monophasic and biphasic) using ruthenium-ion-catalyzed oxidation (RICO). RICO reduces the aromaticity of the polyaromatic core of the molecule in a controlled manner by selective oxidative ring opening. Moreover, the nature of the solvent system determines the product type and distribution, for molecules with more than two aromatic rings. Competitive oxidation between substrates with different numbers of aromatic rings has been studied in detail. It was found that the rate of polyaromatic hydrocarbon oxidation increases with the number of fused aromatic rings. A similar trend was also identified for alkylated aromatic hydrocarbons. The proof-of-concept investigation provides new insight into selective oxidation chemistry for upgrading of polyaromatic molecules.

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