84367-19-1 Usage
Uses
Used in Pharmaceutical Industry:
(S)-3-Hydroxy-1-(3-hydroxy-4-methoxybenzoyl)-2-pyrrolidinone is used as a potential therapeutic agent for the treatment of inflammatory conditions due to its anti-inflammatory properties. The presence of the pyrrolidinone structure in the compound contributes to its ability to mitigate inflammation.
Used in Antioxidant Applications:
In the field of antioxidant research and development, (S)-3-Hydroxy-1-(3-hydroxy-4-methoxybenzoyl)-2-pyrrolidinone is used as a potent antioxidant agent. The hydroxy and methoxy groups on the benzoyl moiety play a significant role in its antioxidant activity, making it a candidate for applications aimed at combating oxidative stress and related diseases.
Used in Drug Delivery Systems:
(S)-3-Hydroxy-1-(3-hydroxy-4-methoxybenzoyl)-2-pyrrolidinone may also be utilized in the development of novel drug delivery systems. Its pharmaceutical properties could be harnessed to improve the delivery, bioavailability, and therapeutic outcomes of various drugs, particularly those targeting inflammatory and oxidative stress-related conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 84367-19-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,3,6 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 84367-19:
(7*8)+(6*4)+(5*3)+(4*6)+(3*7)+(2*1)+(1*9)=151
151 % 10 = 1
So 84367-19-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H13NO5/c1-18-10-3-2-7(6-9(10)15)11(16)13-5-4-8(14)12(13)17/h2-3,6,8,14-15H,4-5H2,1H3/t8-/m0/s1
84367-19-1Relevant academic research and scientific papers
(R,S)-1-(3-Hydroxy-4-methoxybenzoyl)-3-hydroxy-2-pyrrolidinone intermediates therefor and use for treating cerebral insufficiency
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, (2008/06/13)
1-(3-Hydroxy-4-methoxybenzoyl)-3-hydroxy-2-pyrrolidinone of the formula STR1 suitable for the control or prevention of cerebral insufficiency is described. The compound contains an asymmetric carbon atom. Therefore, the two optically active enantiomeric f
