17354-63-1 Usage
Description
1-(P-METHOXYPHENYL)2-NITROPROPENE, also known as PM2NP, is an organic chemical compound that serves as a crucial intermediate in the synthesis of various pharmaceuticals. It is characterized by its molecular structure, which includes a p-methoxyphenyl group and a nitro group attached to a propene backbone. 1-(P-METHOXYPHENYL)2-NITROPROPENE plays a significant role in the development of designer drugs and has potential applications in the pharmaceutical industry.
Uses
1. Used in Pharmaceutical Synthesis:
1-(P-METHOXYPHENYL)2-NITROPROPENE is used as an intermediate in the synthesis of 4-Methoxyamphetamine Hydrochloride (M261015), which is a designer drug belonging to the amphetamine class. This designer drug is known for its ability to release 5-hydroxytryptamine (serotonin) in brain tissue, making it a subject of interest for researchers and pharmaceutical companies.
2. Used in the Amphetamine Industry:
In the amphetamine industry, 1-(P-METHOXYPHENYL)2-NITROPROPENE is used as a key component in the production of 4-Methoxyamphetamine Hydrochloride. 1-(P-METHOXYPHENYL)2-NITROPROPENE is valuable for its potential effects on the central nervous system, particularly its influence on serotonin levels. The development and study of such designer drugs can lead to a better understanding of the mechanisms underlying various neurological and psychiatric disorders, as well as the discovery of new therapeutic approaches.
3. Used in Research and Development:
1-(P-METHOXYPHENYL)2-NITROPROPENE is also utilized in research and development for its potential applications in the creation of new drugs and pharmaceuticals. Its unique molecular structure allows for further modification and exploration of its properties, which could lead to the discovery of novel compounds with specific therapeutic effects.
Check Digit Verification of cas no
The CAS Registry Mumber 17354-63-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,5 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17354-63:
(7*1)+(6*7)+(5*3)+(4*5)+(3*4)+(2*6)+(1*3)=111
111 % 10 = 1
So 17354-63-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO3/c1-8(11(12)13)7-9-3-5-10(14-2)6-4-9/h3-7H,1-2H3
17354-63-1Relevant articles and documents
Reactions of 1-Aryl-1,2-dibromo-2-nitropropanes with 2-Nitro-2-propyl Anion in DMSO
Cho, Bong Rae,Suh, Young Sung,Lee, Seung Jae,Cho, Eun Jeong
, p. 3681 - 3682 (1994)
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A diversity-oriented synthesis of polyheterocycles: Via the cyclocondensation of azomethine imine
Ansari, Arshad J.,Pathare, Ramdas S.,Kumawat, Anita,Maurya, Antim K.,Verma, Sarika,Agnihotri, Vijai K.,Joshi, Rahul,Metre, Ramesh K.,Sharon, Ashoke,Pardasani,Sawant, Devesh M.
supporting information, p. 13721 - 13724 (2019/09/16)
Pd-Catalyzed sequential reactions to afford skeletally diverse molecules are described. The reaction involved azomethine imine formation and a cyclocondensation reaction as individual steps. The methodology provides excellent regio- and stereocontrol. Skeletal diversity was ensured by changing the electrophilic counterpart of azomethine imine. Due to its broader diversity and complexity, the DOS methodology is likely to benefit drug discovery and development in the future.
METHODS AND COMPOSITIONS FOR SELECTIVE AND TARGETED CANCER THERAPY
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Page/Page column 228, (2015/03/28)
Provided herein are methods and compositions for selective and targeted cancer therapy, in particular certain benzothiophenes, benzothiazoles, oxalamides, N-acyl ureas and chromones, and their use in selectively treating certain adenocarcinomas. In some embodiments, the selective toxicity of the compounds may be mediated through SCD1 and/or CYP450 such as CYP4F11.
