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N-(Morpholinomethyl)-2-phenylsuccinimide is a succinimide derivative featuring a morpholine group and a phenyl ring attached to its core. It is a chemical compound utilized in pharmaceutical research and development, known for its unique structure and potential pharmacological activities. N-(Morpholinomethyl)-2-phenylsuccinimide holds promise as a pharmaceutical intermediate in the synthesis of various drugs and is under investigation for its possible biological properties and applications in medicine.

3780-76-5

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3780-76-5 Usage

Uses

Used in Pharmaceutical Research and Development:
N-(Morpholinomethyl)-2-phenylsuccinimide is used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique structure and potential pharmacological activities make it a valuable compound in the development of new medications.
Used in Drug Synthesis:
In the pharmaceutical industry, N-(Morpholinomethyl)-2-phenylsuccinimide is employed as a key component in the creation of novel drug molecules. Its versatility in chemical reactions allows for the design and synthesis of a wide range of therapeutic agents.
Used in Biological Research:
N-(Morpholinomethyl)-2-phenylsuccinimide is also used in biological research to explore its potential biological properties. Further studies are being conducted to understand its interactions with biological systems and its possible applications in medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 3780-76-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,8 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3780-76:
(6*3)+(5*7)+(4*8)+(3*0)+(2*7)+(1*6)=105
105 % 10 = 5
So 3780-76-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H18N2O3/c18-14-10-13(12-4-2-1-3-5-12)15(19)17(14)11-16-6-8-20-9-7-16/h1-5,13H,6-11H2

3780-76-5Relevant academic research and scientific papers

Design, synthesis and anticonvulsant properties of new N-Mannich bases derived from 3-phenylpyrrolidine-2,5-diones

Kamiński, Krzysztof,Obniska, Jolanta,Chlebek, Iwona,Wiklik, Beata,Rzepka, Sabina

, p. 6821 - 6830 (2013/10/22)

The synthesis and anticonvulsant properties of new N-Mannich bases of 3-phenyl- (9a-d), 3-(2-chlorophenyl)- (10a-d), 3-(3-chlorophenyl)- (11a-d) and 3-(4-chlorophenyl)-pyrrolidine-2,5-diones (12a-d) were described. The key synthetic strategies involve the

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