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3-Azetidinecarboxamide, also known as 3-Azabicyclo[3.1.0]hexane-2-carboxamide, is a chemical compound with the molecular formula C4H8N2O. It is a cyclic amide featuring a four-membered ring structure, known for its role in the synthesis of various pharmaceutical compounds. 3-AZETIDINECARBOXAMIDE has been investigated for its potential biological activities and has demonstrated promise as a building block in the development of new drugs. Additionally, it serves as a reagent in organic synthesis and as a starting material for the preparation of more complex molecules. 3-Azetidinecarboxamide is an important intermediate in the production of various pharmaceuticals and biologically active compounds, establishing its value and versatility in the field of medicinal chemistry.

740768-99-4

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740768-99-4 Usage

Uses

Used in Pharmaceutical Synthesis:
3-Azetidinecarboxamide is used as a key intermediate for the synthesis of various pharmaceutical compounds. Its unique cyclic structure and reactivity make it a valuable component in the development of new drugs with potential therapeutic applications.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 3-Azetidinecarboxamide is utilized as a building block for the design and synthesis of novel drug candidates. Its potential biological activities have been a subject of investigation, contributing to the advancement of drug discovery and development.
Used in Organic Synthesis:
3-Azetidinecarboxamide also serves as a reagent in organic synthesis, where it can be employed to form more complex molecules. Its properties allow for various chemical reactions, expanding its utility in the synthesis of organic compounds.
Used in the Preparation of Biologically Active Compounds:
As an intermediate, 3-Azetidinecarboxamide is instrumental in the preparation of biologically active compounds. Its incorporation into these molecules can enhance their efficacy, selectivity, or other pharmacological properties, making it a crucial component in the creation of innovative therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 740768-99-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,0,7,6 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 740768-99:
(8*7)+(7*4)+(6*0)+(5*7)+(4*6)+(3*8)+(2*9)+(1*9)=194
194 % 10 = 4
So 740768-99-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H8N2O/c5-4(7)3-1-6-2-3/h3,6H,1-2H2,(H2,5,7)

740768-99-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name azetidine-3-carboxamide

1.2 Other means of identification

Product number -
Other names 3-AZETIDINECARBOXAMIDE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:740768-99-4 SDS

740768-99-4Relevant academic research and scientific papers

NOVEL TETRAHYDROPYRIDOPYRIMIDINES FOR THE TREATMENT AND PROPHYLAXIS OF HBV INFECTION

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Page/Page column 99; 100, (2018/09/25)

The present invention provides novel compounds having general formula (I), wherein R1 to R4, A, W, Q and Y are as described herein, compositions including the compounds and methods of using the compounds.

Novel potent antagonists of human neuropeptide Y Y5 receptors. Part 2: Substituted benzo[a]cycloheptene derivatives

Itani, Hiromichi,Ito, Harunobu,Sakata, Yoshihiko,Hatakeyama, Yoshifumi,Oohashi, Hiroko,Satoh, Yoshinari

, p. 757 - 761 (2007/10/03)

Novel benzo[a]cycloheptene derivatives were prepared for the purpose of searching new neuropeptide Y-Y5 (NPY-Y5) receptor antagonists. The structure-activity relationships are described and compound 2o (FR226928) showed the most potent affinity for Y5 receptor of all we prepared and was found to have higher potency and better selectivity for Y5 over Y1 receptor affinities when compared with the known lead compound 1.

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