170804-78-1 Usage
Uses
Used in Pharmaceutical Development:
(4-Benzyl-morpholin-2-yl)-acetic acid hydrochloride is used as an intermediate in the synthesis of various pharmaceutical compounds for its potential medicinal properties. Its unique structure, which includes a benzyl group and a morpholine ring, may contribute to the development of new drugs with specific therapeutic effects.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (4-Benzyl-morpholin-2-yl)-acetic acid hydrochloride is used as a building block for the design and synthesis of novel bioactive molecules. Its structural features may allow for the creation of compounds with targeted interactions with biological receptors or enzymes, potentially leading to the discovery of new therapeutic agents.
Used in Central Nervous System Therapeutics:
Due to its structural similarity to certain neurotransmitters or receptors, (4-Benzyl-morpholin-2-yl)-acetic acid hydrochloride may be used as a starting point for the development of drugs aimed at treating central nervous system disorders. Its potential therapeutic effects could be explored in the context of neurological conditions, mental health disorders, or cognitive functions.
Used in Pharmaceutical Formulation:
The hydrochloride form of (4-Benzyl-morpholin-2-yl)-acetic acid may be used to improve the solubility and stability of the compound in pharmaceutical formulations. This enhancement can facilitate the development of more effective drug delivery systems, ensuring that the compound reaches its target site in the body with optimal bioavailability and minimal side effects.
Check Digit Verification of cas no
The CAS Registry Mumber 170804-78-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,8,0 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 170804-78:
(8*1)+(7*7)+(6*0)+(5*8)+(4*0)+(3*4)+(2*7)+(1*8)=131
131 % 10 = 1
So 170804-78-1 is a valid CAS Registry Number.
170804-78-1Relevant academic research and scientific papers
Synthsis and gastroprokinetic activity of N-(4-amino-5-chloro-2-methoxyphenyl)-4-benzyl-2-morpholineacetamide and related compounds
Kato, S.,Morie, T.,Yoshida, N.,Fujiwara, I.,Kon, T.
, p. 609 - 616 (2007/10/02)
4-Amino-N--5-chloro-2-methoxybenzamide 1a and its 2-ethoxy analogue 1b show a potent gastroprokinetic activity.To examine the effect of reversal of the amide linkage of 1a and 1b, N-(4-amino-5-chloro-2-methoxyphenyl)-4-benzyl-2-morpholineacetamide and related compounds (2 and 8-13) were prepared and evaluated for gastroprokinetic activity by determining their effects on gastric emptying of a phenol red semisolid meal a serotonin-4-receptor binding assay.Reversal of the amide bond resulted in a fall in activity; the amide bond of the 2-morpholinyl benzamides is essential for a potent gastroprokinetic activity.Molecular superimposition of 2c upon 1b using computer graphics suggested that the location of the morpholine ring and N-benzyl group is crucial for the activity. gastroprokinetic activity / 2-morpholineacetamide / molecular-superimposition / mosapride / 2-morpholinyl benzamide
