125773-72-0 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
It serves as a starting material for the synthesis of advanced polymers and plastics with enhanced properties.
Explanation
It belongs to a class of organic compounds that contain an aromatic ring and a nitrile functional group (C≡N).
Explanation
It can be used to create more complex organic molecules by forming new chemical bonds with other compounds.
Explanation
The compound is known for its ability to withstand high temperatures without significant degradation.
Explanation
It exhibits a strong resistance to chemical corrosion, making it suitable for use in harsh environments.
Explanation
Due to its properties, it is valuable in a range of industrial applications, such as manufacturing and materials science.
Explanation
It is used in the production of semiconductors and insulating materials, which are essential components in electronic devices.
Explanation
It poses health risks and should be handled with caution to prevent exposure and potential harm.
Explanation
Careful handling, storage, and disposal are necessary to minimize the risk of exposure and ensure the safety of workers and the environment.
Common use
Precursor in the production of high-performance polymers and plastics
Chemical classification
Aromatic nitrile
Building block
Used in organic synthesis
Heat resistance
High
Chemical corrosion resistance
High
Industrial applications
Various
Utilization in electronics
Manufacturing of electronic components
Toxicity
Can be toxic and hazardous
Safety precautions
Proper management required
Check Digit Verification of cas no
The CAS Registry Mumber 125773-72-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,7,7 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 125773-72:
(8*1)+(7*2)+(6*5)+(5*7)+(4*7)+(3*3)+(2*7)+(1*2)=140
140 % 10 = 0
So 125773-72-0 is a valid CAS Registry Number.
125773-72-0Relevant articles and documents
Phase transition, optical and photoconductive properties of bay-substituted benzoporphyrin derivatives
Liu, Xu-Ying,Usui, Takayuki,Iino, Hiroaki,Hanna, Jun-Ichi
, p. 8186 - 8193 (2013)
Two benzoporphyrin derivatives substituted with long side chains at the bay positions have been synthesized through a facile route. They were confirmed to show two separate columnar phases upon cooling, i.e., a hexagonal columnar phase and a rectangular columnar phase. In particular, the temperature dependence of the electronic spectra revealed that the Q-band split into two peaks, indicating the existence of typical herringbone-type dimers. Moreover, their photoconductive properties were studied by steady-state and transient photocurrent measurements. It was found that both benzoporphyrins exhibited very fast hole mobility over 0.1 cm2 V-1 s-1 in both columnar phases and a high charge carrier generation efficiency up to 2%, demonstrating that they are potential p-type organic semiconductors for photovoltaic devices.
Catalytic epoxidation of stilbenes with non-peripherally alkyl substituted carbonyl ruthenium phthalocyanine complexes
Enow, Charles A.,Marais, Charlene,Bezuidenhoudt, Barend C.B.
experimental part, p. 403 - 412 (2012/08/07)
A number of novel carbonyl(1,4,8,11,15,18,22,25-octaalkylphthalocyaninato)- ruthenium(II) complexes were prepared by metal insertion with Ru 3(CO)12. The new compounds have been characterized by 1H NMR, 13C NMR, IR, UV-vis and mass spectroscopy. This study demonstrated that this type of complexes and specifically carbonyl(1,4,8,11,15,18,22,25-octahexylphthalo-cyaninato)ruthenium(II) and carbonyl[1,4,8,11,15,18,22,25-octa(2-cyclohexylethyl)phthalocyaninato] -ruthenium(II), exhibit high catalytic activity and stability in the epoxidation of stilbenes with 2,6-dichloropyridine N-oxide as oxidant.
