94375-26-5 Usage
Uses
Used in Organic Chemical Synthesis:
[4-(4-bromophenyl)phenyl] benzoate is used as a building block in the synthesis of various organic compounds. Its unique structure allows it to serve as a valuable intermediate in the creation of complex molecules, contributing to the development of new materials and substances.
Used in Pharmaceutical Production:
In the pharmaceutical industry, [4-(4-bromophenyl)phenyl] benzoate is utilized as a key component in the development of different drugs. Its presence in the molecular structure can influence the properties and efficacy of the final product, making it an essential element in drug design and formulation.
Used in Agrochemical Production:
[4-(4-bromophenyl)phenyl] benzoate also finds application in the agrochemical sector, where it is employed in the synthesis of various agrochemicals. These can include pesticides, herbicides, and other chemicals used in agriculture to enhance crop protection and yield.
Used in Specialty Chemicals:
[4-(4-bromophenyl)phenyl] benzoate is also used in the production of specialty chemicals, which are tailored for specific industries and applications. The versatility of [4-(4-bromophenyl)phenyl] benzoate allows it to contribute to the development of unique chemical products that cater to the needs of various markets.
Check Digit Verification of cas no
The CAS Registry Mumber 94375-26-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,3,7 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 94375-26:
(7*9)+(6*4)+(5*3)+(4*7)+(3*5)+(2*2)+(1*6)=155
155 % 10 = 5
So 94375-26-5 is a valid CAS Registry Number.
94375-26-5Relevant academic research and scientific papers
Syntheses and photophysical properties of some 4-arylpyridinium salts
Kelley,Ansu,Budisusetyo,Ghiorghis,Qin,Kauffman
, p. 11 - 23 (2007/10/03)
A number of 4-arylpyridines, many methoxy substituted, were prepared by an efficient two-step method involving aryl Grignard addition to 1-methyl-4-piperidone and direct aromatization of the resulting 4-aryl-4-piperidinols. The pyridines were N-alkylated to give sulfonate salts desired for their fluorescent properties. Study of selected compounds as laser dyes revealed several structures to be efficient dyes lasing in the 530-550 nm range. Two new diazaquaterphenyls were prepared and were quaternized. These salts exhibited intense fluorescence in the 420-450 nm range, but would not lase. A phenolic azaterphenyl suitably substituted for excited state intramolecular proton transfer (ESIPT) did not fluoresce at all.
