149340-93-2 Usage
Description
N-[2-(4-Nitrophenyl)ethyl]-N'-propylurea is a synthetic, organic compound that features a urea backbone chemically bonded to a nitrophenyl group and a propyl chain. The presence of the nitrophenyl and ethyl groups suggests it may exhibit unique optical properties, although its specific applications and characteristics are not extensively documented in scientific literature. Like other urea compounds, it may have potential industrial uses such as solvents, detergents, or as a chemical intermediate for pharmaceuticals and other chemicals. However, the nitrophenyl group may also impart explosive or reactive properties, necessitating careful handling. Further study and a comprehensive understanding of this chemical structure are required to ascertain its potential applications.
Uses
Used in Chemical Intermediates:
N-[2-(4-Nitrophenyl)ethyl]-N'-propylurea is used as a chemical intermediate for the synthesis of various pharmaceuticals and other chemicals. Its urea backbone and nitrophenyl group provide a versatile structure that can be further modified or used as a building block in the production of more complex molecules.
Used in Solvents and Detergents:
N-[2-(4-Nitrophenyl)ethyl]-N'-propylurea is used as a component in solvents and detergents, where its urea backbone and nitrophenyl group may contribute to the solubility and cleaning properties of the formulations.
Used in Optical Applications:
Due to the presence of the nitrophenyl and ethyl groups, N-[2-(4-Nitrophenyl)ethyl]-N'-propylurea may be used in optical applications, potentially exploiting its unique optical properties for use in materials science or photonics.
Used in Explosive Compounds:
The nitrophenyl group in N-[2-(4-Nitrophenyl)ethyl]-N'-propylurea may lead to explosive or reactive properties, making it a candidate for use in the development of explosive compounds. However, this application requires careful handling and further study to ensure safety and effectiveness.
Note: The potential uses mentioned above are speculative and based on the chemical structure of N-[2-(4-Nitrophenyl)ethyl]-N'-propylurea. Further research and development are necessary to confirm these applications and to explore any additional uses that may exist.
Check Digit Verification of cas no
The CAS Registry Mumber 149340-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,3,4 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 149340-93:
(8*1)+(7*4)+(6*9)+(5*3)+(4*4)+(3*0)+(2*9)+(1*3)=142
142 % 10 = 2
So 149340-93-2 is a valid CAS Registry Number.
149340-93-2Relevant articles and documents
A1 ADENOSINE RECEPTOR ANTAGONISTS
-
Page 17-19, (2010/02/08)
Compounds of the general formula (I) are described wherein A is a 5- or 6-membered aromatic or heteroaromatic ring. Compositions comprising such compounds and methods of use thereof are also described.
Adenosine A1 antagonists. 3. Structure-activity relationships on amelioration against scopolamine- or N6-((R)-phenylisopropyl)adenosine-induced cognitive disturbance.
Suzuki,Shimada,Shiozaki,Ichikawa,Ishii,Nakamura,Nonaka,Kobayashi,Fuse
, p. 2508 - 2518 (2007/10/02)
The effects of a variety of adenosine A1 and A2 antagonists on N6-((R)-phenylisopropyl)adenosine (R-PIA)- and scopolamine-induced amnesias were investigated in rodents in order to clarify the role of adenosine receptors in learning and memory. Some of the
