1104074-27-2 Usage
Derivative of phenylalanine
2-(1,3-dioxo-1,3,3a,4,7,7a-hexahydro-2H-isoindol-2-yl)-3-phenylpropanoic acid is derived from the amino acid phenylalanine, which is an essential amino acid that plays a role in the production of neurotransmitters in the brain.
Building block for drug synthesis
2-(1,3-dioxo-1,3,3a,4,7,7a-hexahydro-2H-isoindol-2-yl)-3-phenylpropanoic acid is commonly used in the pharmaceutical industry as a building block for the synthesis of various drugs, particularly those that target the central nervous system.
Potential therapeutic agent for cognitive disorders
2-(1,3-dioxo-1,3,3a,4,7,7a-hexahydro-2H-isoindol-2-yl)-3-phenylpropanoic acid has been studied for its potential as a therapeutic agent for the treatment of cognitive disorders, such as Alzheimer's disease, due to its ability to modulate neurotransmitter levels in the brain.
Anti-inflammatory and analgesic properties
In addition to its potential as a therapeutic agent for cognitive disorders, 2-(1,3-dioxo-1,3,3a,4,7,7a-hexahydro-2H-isoindol-2-yl)-3-phenylpropanoic acid has also been studied for its anti-inflammatory and analgesic properties, making it a versatile compound with a wide range of potential applications in medicine and drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 1104074-27-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,4,0,7 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1104074-27:
(9*1)+(8*1)+(7*0)+(6*4)+(5*0)+(4*7)+(3*4)+(2*2)+(1*7)=92
92 % 10 = 2
So 1104074-27-2 is a valid CAS Registry Number.
1104074-27-2Relevant academic research and scientific papers
Firstova,Kofanov,Zakshevskaya,Kovaleva
, p. 204 - 213 (2019)
A method for the high-yield synthesis of several amides of carboxylic acids containing an imide, a cyclohexene, and a norbornene cycle as well as fragments of natural amino acids has been developed. The compounds synthesized have been tested for mutagenic activity on plant objects using the Allium test. It has been shown that the presence of a nitro group endows the compound with inhibitory property and the capacity to induce chromosomal rearrangements, whereas the presence of an aliphatic carbon chain, a methyl group, and a morpholine fragment, on the contrary, confers growth-regulating properties without inducing the mutagenic effect. The study has confirmed that the resulting biologically active compounds are of interest for practical implementation in agriculture.
