Welcome to LookChem.com Sign In|Join Free
  • or
1,2,4-Benzenetricarboxylic acid, 5-bromo-, trimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13124-85-1

Post Buying Request

13124-85-1 Suppliers

Recommended suppliers

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

13124-85-1 Usage

Family

Benzenetricarboxylic acid derivatives

Formation

Ester formed by the reaction of 1,2,4-benzenetricarboxylic acid with bromine and trimethyl alcohol

Common Uses

Production of polymers and resins
Manufacturing of pharmaceuticals and agrochemicals

Potential Applications

Flame retardant
Plasticizer in various industrial processes

Safety Precautions

May cause skin and eye irritation
Respiratory issues if inhaled

Handling

Handle with care to avoid exposure and potential health risks

Check Digit Verification of cas no

The CAS Registry Mumber 13124-85-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,2 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13124-85:
(7*1)+(6*3)+(5*1)+(4*2)+(3*4)+(2*8)+(1*5)=71
71 % 10 = 1
So 13124-85-1 is a valid CAS Registry Number.

13124-85-1Downstream Products

13124-85-1Relevant academic research and scientific papers

Electron-Poor Thiophene 1,1-Dioxides: Synthesis, Characterization, and Application as Electron Relays in Photocatalytic Hydrogen Generation

Tsai, Chia-Hua,Chirdon, Danielle N.,Kagalwala, Husain N.,Maurer, Andrew B.,Kaur, Aman,Pintauer, Tomislav,Bernhard, Stefan,Noonan, Kevin J. T.

, p. 11517 - 11524 (2015)

The synthesis and characterization of electron-poor thiophene 1,1-dioxides bearing cyanated phenyl groups are reported. The electron-accepting nature of these compounds was evaluated by cyclic voltammetry, and highly reversible and facile reductions were observed for several derivatives. Moreover, some of the reduced thiophene dioxides form colorful anions, which were investigated spectroelectrochemically. Photoluminescence spectra of the electron-deficient sulfones were measured in CH2Cl2, and they emit in the blue-green region with significant variation in the quantum yield depending on the aryl substituents. By expanding the degree of substitution on the phenyl rings, quantum yields up to 34% were obtained. X-ray diffraction data are reported for two of the thiophene 1,1-dioxides, and the electronic structure was probed for all synthesized derivatives through DFT calculations. The dioxides were also examined as electron relays in a photocatalytic water reduction reaction, and they showed potential to boost the efficiency.

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 13124-85-1