Welcome to LookChem.com Sign In|Join Free
  • or
[1,1',3',1",3",1"'-Quaterphenyl]-3,3'''-dicarbonaldehyde is a chemical compound with the molecular formula C52H34O2. It is a dicarbonaldehyde derivative of quaterphenyl, a polycyclic aromatic hydrocarbon. [1,1',3',1",3",1"'-Quaterphenyl]-3,3'''-dicarbonaldehyde is characterized by its unique structure and potential applications in various fields.

127404-22-2

Post Buying Request

127404-22-2 Suppliers

Recommended suppliers

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

127404-22-2 Usage

Uses

Used in Organic Synthesis:
[1,1',3',1",3",1"'-Quaterphenyl]-3,3'''-dicarbonaldehyde is used as a building block in organic synthesis for the creation of various organic compounds and polymers. Its unique structure allows for the formation of complex molecules with specific properties.
Used in Material Science:
In the field of material science, [1,1',3',1",3",1"'-Quaterphenyl]-3,3'''-dicarbonaldehyde is utilized for the development of advanced materials. Its potential applications include the synthesis of liquid crystals, organic semiconductors, and optoelectronic devices, where its structural features contribute to the desired material properties.
Used as a Fluorescent Probe in Biochemistry and Cell Biology:
[1,1',3',1",3",1"'-Quaterphenyl]-3,3'''-dicarbonaldehyde may also be employed as a fluorescent probe for studies in biochemistry and cell biology. Its optical properties can be harnessed to investigate biological processes and interactions at the molecular level.

Check Digit Verification of cas no

The CAS Registry Mumber 127404-22-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,4,0 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 127404-22:
(8*1)+(7*2)+(6*7)+(5*4)+(4*0)+(3*4)+(2*2)+(1*2)=102
102 % 10 = 2
So 127404-22-2 is a valid CAS Registry Number.

127404-22-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1-Imidazolyl)benzaldehyde

1.2 Other means of identification

Product number -
Other names 3-imidazol-1-ylbenzaldehyde

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:127404-22-2 SDS

127404-22-2Relevant academic research and scientific papers

Ultrafast singlet - singlet energy transfer in self-assembled via metal - ligand axial coordination of free-base porphyrin - zinc phthalocyanine and free-base porphyrin - zinc naphthalocyanine Dyads

Maligaspe, Eranda,Kumpulainen, Tatu,Lemmetyinen, Helge,Tkachenko, Nikolai V.,Subbaiyan, Navaneetha K.,Zandler, Melvin E.,D'Souza, Francis

, p. 268 - 277 (2010)

Singlet - singlet energy transfer in self-assembled via axial coordination of imidazole-appended (at different positions of one of the meso-phenyl entities) free-base tetraphenylporphyrin, H2PIm, to either zinc phthalocyanine, ZnPc, or zinc nap

P2X4 RECEPTOR MODULATING COMPOUNDS

-

Paragraph 00248, (2015/06/25)

Provided herein are P2X4 receptor modulating compounds, methods of their synthesis, pharmaceutical compositions comprising the compounds, and methods of their use. The compounds provided herein are useful for the treatment, prevention, and/or management of various disorders, including but not limited to, chronic pain, neuropathy, inflammatory diseases and central nervous system disorders.

Magnetically retrievable lepidocrocite supported copper oxide nanocatalyst (Fe-CuO) for N-arylation of imidazole

Sivakami,Babu, S. Ganesh,Dhanuskodi,Karvembu

, p. 8571 - 8578 (2015/03/03)

A simple and efficient lepidocrocite-supported copper oxide catalyst (Fe-CuO) has been successfully prepared by a simple precipitation method in aqueous medium from readily available inexpensive starting materials and was used as a heterogeneous nanocatal

Synthesis and characterization of Sant-75 derivatives as Hedgehog-pathway inhibitors

Che, Chao,Li, Song,Yang, Bo,Xin, Shengchang,Yu, Zhixiong,Shao, Taofeng,Tao, Chuanye,Lin, Shuo,Yang, Zhen

scheme or table, p. 841 - 849 (2012/07/28)

Sant-75 is a newly identified potent inhibitor of the hedgehog pathway. We designed a diversity-oriented synthesis program, and synthesized a series of Sant-75 analogues, which lays the foundation for further investigation of the structure-activity relationship of this important class of hedgehog-pathway inhibitors.

Imidazol-1-yl and Pyridin-3-yl Derivatives of 4-Phenyl-1,4-dihydropyridines Combining Ca2+ Antagonism and Thromboxane A2 Synthase Inhibition

Cozzi, Paolo,Carganico, Germano,Fusar, Domenico,Grossoni, Mauro,Menichincheri, Maria,et al.

, p. 2964 - 2972 (2007/10/02)

A series of derivatives of 4-phenyl-1,4-dihydropyridine bearing imidazol-1-yl or pyridin-3-yl moieties on the phenyl ring were synthesized with the aim of combining Ca2+ antagonism and thromboxane A2 (Tx A2) synthase inhib

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 127404-22-2