134050-75-2 Usage
Uses
Used in Pharmaceutical Synthesis:
Methyl 5-morpholino-2-nitrobenzenecarboxylate is utilized as a key intermediate in the production of various pharmaceuticals. Its unique structure allows for the creation of a wide range of medicinal compounds, contributing to the development of new treatments and therapies.
Used in Organic Chemistry Research:
As a building block in organic chemistry, methyl 5-morpholino-2-nitrobenzenecarboxylate is employed in research to explore novel chemical reactions and syntheses. Its presence in the development of new organic compounds can lead to advancements in material science, chemical engineering, and related fields.
Used in Anti-inflammatory and Analgesic Applications:
Methyl 5-morpholino-2-nitrobenzenecarboxylate has been studied for its potential to exhibit anti-inflammatory and analgesic properties. If these properties are confirmed, the compound could be used in the development of new medications aimed at reducing inflammation and pain.
Used in Industrial Applications:
methyl 5-morpholino-2-nitrobenzenecarboxylate's versatility and reactivity make it suitable for use in various industrial processes. It can be incorporated into the production of specialty chemicals, coatings, and other materials where its unique properties can be leveraged to enhance performance or create new functionalities.
Check Digit Verification of cas no
The CAS Registry Mumber 134050-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,0,5 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 134050-75:
(8*1)+(7*3)+(6*4)+(5*0)+(4*5)+(3*0)+(2*7)+(1*5)=92
92 % 10 = 2
So 134050-75-2 is a valid CAS Registry Number.
134050-75-2Relevant academic research and scientific papers
QUINAZOLINONE AND PYRIDOPYRIMIDINE A-II ANTAGONISTS
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, (2008/06/13)
Substituted quinazolinones and pyridopyrimidines of structural formula 1 STR1 are angiotensin II antagonists useful in the treatment of disorders related to the reninangiotensin system (RAS) such as hypertension, congestive heart failure, ocular hypertension and certain CNS disorders.
QUINAZOLINONES AND PYRIDOPYRIMIDINONES
-
, (2008/06/13)
Substituted quinazolinones and pyridopyrimidines of structural formula I STR1 are angiotensin II antagonists useful in the treatment of disorders related to the renin-angiotensin system (RAS) such as hypertension, congestive heart failure, ocular hypertension and certain CNS disorders.
3H-azepines and related systems. Part 4. Preparation of 3 H-azepin-2-ones and 6H-azepino[2,1-b]quinazolin-12-ones by photo-induced ring expansions of aryl azides
Lamara, Kaddour,Smalley, Robert K.
, p. 2277 - 2290 (2007/10/02)
Photolysis of a series of p-substituted phenyl azides (p-X-C6H4N3; X= CO2Me, CO2Et, CN, CF3, SO2NH2, CO2CHPh2, COMe, CHO, and NO2) in 1:1 (v/v) THF-water solution produces, in the majority of cases, a 5-substituted-3H-azepine-2-one. In a like manner, 3H-azepin-2-one-3-carboxylates can be prepared from 5-substituted-2-azidobenzoates, providing the 5-substituent is electron-withdrawing. 3H-Azepin-2-one mono- and di-carboxylic acids, the former in admixture with decarboxylated material, and 6H-azepino[2,1-b]quinazolin-12-ones, are obtained by irradiation of 2-azidobenzoic acid and of 5-azidoisophthalic acid, respectively. The mode of formation of the azepino-quinazolinones is discussed.
