Welcome to LookChem.com Sign In|Join Free
  • or
3,4,5,6-tetrafluorophthaloyl dichloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14900-74-4

Post Buying Request

14900-74-4 Suppliers

Recommended suppliers

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

14900-74-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14900-74-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,0 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14900-74:
(7*1)+(6*4)+(5*9)+(4*0)+(3*0)+(2*7)+(1*4)=94
94 % 10 = 4
So 14900-74-4 is a valid CAS Registry Number.

14900-74-4Relevant academic research and scientific papers

X-ray diffraction and theoretical studies for the quantitative assessment of intermolecular arene-perfluoroarene stacking interactions

Bacchi, Sergio,Benaglia, Maurizio,Cozzi, Franco,Demartin, Francesco,Filippini, Giuseppe,Gavezzotti, Angelo

, p. 3538 - 3546 (2006)

The arene-perfluoroarene stacking interaction was studied by experimental and theoretical methods. A series of compounds with different possibilities for formation of this recognition motif in the solid state were synthesized, and their crystal structures

Revisiting phosphorus analogues of phthalimides and naphthalimides: Syntheses and comparative studies

Takeda, Youhei,Nishida, Takuya,Hatanaka, Kota,Minakata, Satoshi

, p. 1666 - 1672 (2015)

A series of phosphorus analogues of aromaticfused monoimides (phthalimides and naphthalimides) bearing a mesityl group on the P center have been synthesized. In a comparison of their photophysical, electrochemical, and thermal properties with those of the corresponding imides, the impact of P incorporation was revealed. Furthermore, theoretical studies using DFT methods were conducted to understand their properties.

Assembly Pattern of Supramolecular Hydrogel Induced by Lower Critical Solution Temperature Behavior of Low-Molecular-Weight Gelator

Wu, Shuanggen,Zhang, Qiao,Deng, Yan,Li, Xing,Luo, Zheng,Zheng, Bo,Dong, Shengyi

supporting information, p. 448 - 455 (2020/01/09)

Although the gelation process and lower critical solution temperature (LCST) behavior are well acknowledged in polymer systems, low-molecular-weight gelators (LMWGs) rarely display LCST behavior during supramolecular gelation. Herein, we report an LMWG system with LCST-type thermoresponsiveness and an LCST-triggered supramolecular gelation process. Temperature plays a crucial role in this system, not only affecting the LCST phase separation but also triggering the gelation process. The backbones (three-dimensional structures) of the resulting hydrogel are the hierarchical assemblies of the LMWG undergoing the LCST phase separation. Hence, the gelation of the LMWG is only realized when the gelation temperature is above the critical transition temperature (Tcloud) of the LCST behavior, which is different from many supramolecular or polymeric hydrogel systems.

Grignard Reactions on Ortho Dicarboxylic Arene Derivatives. Synthesis of 1,3-Dithienylisothianaphthene Compounds

Kiebooms, Rafa?l H. L.,Adriaensens, Peter J. A.,Vanderzande, Dirk J. M.,Gelan, Jan M. J. V.

, p. 1473 - 1480 (2007/10/03)

1,3-Dithienylisothianaphthene (10a) is obtained through ring closure of 1,2-dithienoylbenzene (7a). The synthesis of 7a has been accomplished based on a Grignard reaction by adding 2-thiophene-magnesium bromide to 1,2-di(S-(2-pyridinyl)) benzenedithioate (6b) to obtain 7a in a yield of 95%. The use of 6b avoids the formation of the corresponding 3,3-dithienyl-3H-isobenzofuran-1(3H)-one (dithienylphthalide, 8). The same procedure is applied to obtain 1,3-dithienyl-4,5,6,7-tetradeuterioisothianaphthene (10b) and 1,3-dithienyl-4,5,6,7-tetrafluoroisothianaphthene (10c). The synthesis of the 2,3-dithienoylpyridine (12a), 3,4-dithienoylpyridine (12b), and 2,3-dithienoylpyrazine (12c) however fails. The presence of nitrogen in the central ring system influences the result of the Grignard reaction. Possibly the free electron pair of the nitrogen interferes with the formation of a stable six-membered ring intermediate which is essential for the diketone formation.

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 14900-74-4