89516-42-7 Usage
Description
1-(10H-phenothiazin-2-yl)-3-pyrrolidin-1-ylpropan-1-one is a chemical compound belonging to the phenothiazine class, which is known for its use in antipsychotic medications. 1-(10H-phenothiazin-2-yl)-3-pyrrolidin-1-ylpropan-1-one features a phenothiazine core and a pyrrolidinylpropanone moiety, suggesting its potential as a valuable drug candidate with therapeutic applications. It may exhibit psychoactive and sedative properties, possibly interacting with the central nervous system. Further research and testing are required to determine its full pharmacological profile and potential medical applications.
Uses
Used in Pharmaceutical Industry:
1-(10H-phenothiazin-2-yl)-3-pyrrolidin-1-ylpropan-1-one is used as a potential therapeutic agent for its psychoactive and sedative properties, targeting the central nervous system. Its development could lead to new antipsychotic medications, pending further research and testing to confirm its efficacy and safety.
Used in Research and Development:
In the field of pharmaceutical research and development, 1-(10H-phenothiazin-2-yl)-3-pyrrolidin-1-ylpropan-1-one serves as a valuable compound for studying its interactions with the central nervous system and its potential role in the treatment of psychiatric disorders. This research could contribute to the advancement of antipsychotic drug discovery and development.
Check Digit Verification of cas no
The CAS Registry Mumber 89516-42-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,1 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 89516-42:
(7*8)+(6*9)+(5*5)+(4*1)+(3*6)+(2*4)+(1*2)=167
167 % 10 = 7
So 89516-42-7 is a valid CAS Registry Number.
89516-42-7Relevant articles and documents
Phenothiazine Derivatives as Antiparkinsonian Agents
Kumar, P.,Nath, C.,Agarwal, Jagdish C.,Bhargava, K. P.,Shanker, K.
, p. 952 - 954 (2007/10/02)
2-Acetyl-10-chloroacetylphenothiazine (II) undergoes condensation with substituted amines to yield 2-acetyl-10-(arylalkylaminoacetyl)phenothiazines (III).Mannich reaction of 2-acetylphenothiazine (I) with amines gives 2-(N'-substituted-propanoyl)phenothia
