59741-17-2 Usage
Uses
Used in Pharmaceutical Production:
2-Methoxy-5-nitrophenyl isocyanate is utilized as a key intermediate in the synthesis of various pharmaceuticals. Its reactivity allows for the creation of new compounds with potential therapeutic properties, contributing to the development of novel drugs.
Used in Organic Compound Synthesis:
In the field of organic chemistry, 2-Methoxy-5-nitrophenyl isocyanate serves as a building block for the production of a range of organic compounds. Its ability to form stable amides and urethanes makes it a valuable component in the synthesis of complex organic molecules for various applications.
Used in Research and Development:
2-Methoxy-5-nitrophenyl isocyanate is also employed in research and development settings, where its unique chemical properties are explored for potential applications in new chemical processes or as a precursor to other valuable compounds.
Used in Chemical Education:
In educational institutions, 2-Methoxy-5-nitrophenyl isocyanate can be used as a teaching aid to demonstrate the principles of organic synthesis and the properties of isocyanate derivatives, providing students with hands-on experience in chemical reactions and compound formation.
Check Digit Verification of cas no
The CAS Registry Mumber 59741-17-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,7,4 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 59741-17:
(7*5)+(6*9)+(5*7)+(4*4)+(3*1)+(2*1)+(1*7)=152
152 % 10 = 2
So 59741-17-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N2O4/c1-14-8-3-2-6(10(12)13)4-7(8)9-5-11/h2-4H,1H3
59741-17-2Relevant academic research and scientific papers
5-Hydroxytryptamine (5-HT3) Receptor Antagonists. 3. Ortho-Substituted Phenylureas
Bermudez, Jose,Dabbs, Steven,King, Frank D.
, p. 1932 - 1935 (2007/10/02)
A novel series of potent 5-HT3 receptor antagonists, ortho-substituted phenylureas 6a-z, is described in which the 5-membered ring of the previously reported indazoles and indolines has been replaced by an intramolecular hydrogen bond.High potency was found both for carbamate 6a and urea 6b.Granatane 6c was less potent than the equivalent tropane.Phenylurea 11c lacking the ortho substituent was inactive.Whereas further substitution could not be tolerated in the aromatic ring, activity was retained with a range of O-alkyl groups, compounds 6k-t.In addition, good activity was found for ortho ester 6u and sulfonamide 6x.The ortho-substituted phenylureas can therefore be regarded as bioisosteres of the 6,5-heterocycles indole, indazole, and indoline.
