1503-98-6 Usage
Description
Cyclobutanecarboxamide, also known as cyclobutylcarboxamide, is a chemical compound characterized by the molecular formula C5H9NO. It presents as a white, crystalline solid that exhibits low solubility in water but is readily soluble in organic solvents. Cyclobutanecarboxamide is predominantly utilized as an intermediate in the synthesis of pharmaceuticals and agrochemicals, and it also finds applications in the production of polymers and as a component in organic synthesis processes. Given its low water solubility and potential for bioaccumulation, proper handling and disposal are essential to mitigate any environmental and health concerns.
Uses
Used in Pharmaceutical Industry:
Cyclobutanecarboxamide is used as a key intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, cyclobutanecarboxamide serves as an intermediate for the production of different agrochemicals, aiding in the creation of products that enhance crop protection and yield.
Used in Polymer Manufacturing:
Cyclobutanecarboxamide is utilized in the manufacturing of polymers, where it plays a role in the formation of polymeric materials with specific properties for various applications.
Used in Organic Synthesis:
As a building block in organic synthesis, cyclobutanecarboxamide is employed in the creation of complex organic molecules for a range of uses, including specialty chemicals and advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 1503-98-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,0 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1503-98:
(6*1)+(5*5)+(4*0)+(3*3)+(2*9)+(1*8)=66
66 % 10 = 6
So 1503-98-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NO/c6-5(7)4-2-1-3-4/h4H,1-3H2,(H2,6,7)
1503-98-6Relevant articles and documents
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Hoz,S.,Aurbach,D.
, p. 7685 (1983)
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One-Pot Anodic Conversion of Symmetrical Bisamides of Ethylene Diamine to Unsymmetrical gem-Bisamides of Methylene Diamine
Golub, Tatiana,Dou, Gui-Yuan,Zeng, Cheng-Chu,Becker, James Y.
supporting information, p. 7961 - 7964 (2019/10/11)
Symmetrical bisamides of ethylene diamine of type ArCONHCH2CH2NHCOAr undergo anodic C-C bond cleavage in acetonitrile-LiClO4 under controlled-potential electrolysis. The electrogenerated carbocation intermediates react with the solvent acetonitrile to afford unsymmetrical gem-bisamides of type ArCONHCH2NHCOMe in a one-pot reaction. The yields of the latter products are moderate (up to 60%). Other minor products involve two symmetrical gem-bisamides of type ArCONHCH2NHCOAr and MeCONHCH2NHCOMe and fragmentation products (e.g., ArCONHCHO, ArCONH2, and ArCN).
SUBSTITUTED THIAZOLE OR OXAZOLE P2X7 RECEPTOR ANTAGONISTS
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Page/Page column 39, (2015/09/22)
The present invention refers to novel substituted thiazole and oxazole compounds of formula (I) having P2X7 receptor (P2X7) antagonistic properties. The compounds are useful in the treatment or prophylaxis of diseases associated with P2X7 receptor activity in animals, in particular humans.
