1214741-19-1 Usage
Uses
Used in Pharmaceutical Industry:
3-(1,1-diMethylethyl)dihydro-1,5-dioxo-(3R,7aR)-1H,3H-Pyrrolo[1,2-c]oxazole-7a(5H)-carboxaldehyde is used as a potential pharmaceutical compound for its unique structural features and functional groups. The presence of ketone, aldehyde, and tertiary butyl groups may allow for interactions with biological targets, making it a candidate for drug development.
Used in Chemical Research:
3-(1,1-diMethylethyl)dihydro-1,5-dioxo-(3R,7aR)-1H,3H-Pyrrolo[1,2-c]oxazole-7a(5H)-carboxaldehyde is used as a subject of study in chemical research, particularly in the field of organic chemistry. Its unique structure and functional groups provide opportunities for investigating reaction mechanisms, synthesis pathways, and potential applications in various chemical processes.
Used in Material Science:
3-(1,1-diMethylethyl)dihydro-1,5-dioxo-(3R,7aR)-1H,3H-Pyrrolo[1,2-c]oxazole-7a(5H)-carboxaldehyde may be utilized in material science for the development of new materials with specific properties. 3-(1,1-diMethylethyl)dihydro-1,5-dioxo-(3R,7aR)-1H,3H-Pyrrolo[1,2-c]oxazole-7a(5H)-carboxaldehyde's structural features could contribute to the creation of novel materials with applications in various industries, such as electronics or advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 1214741-19-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,4,7,4 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1214741-19:
(9*1)+(8*2)+(7*1)+(6*4)+(5*7)+(4*4)+(3*1)+(2*1)+(1*9)=121
121 % 10 = 1
So 1214741-19-1 is a valid CAS Registry Number.
1214741-19-1Relevant articles and documents
Collective Total Synthesis of (-)-Lundurines A-C
Xu, Wei,Zhao, Jianfei,Tao, Cheng,Wang, Huifei,Li, Yun,Cheng, Bin,Zhai, Hongbin
, p. 1509 - 1512 (2018)
A collective asymmetric total synthesis of lundurines A-C using l-pyroglutamic acid derived from the chiral pool is described. The key steps include a tandem reductive amination/lactamization sequence to introduce the pyrrolidinone ring, a palladium-catalyzed intramolecular direct C-H vinylation of indole to construct the crucial polyhydroazocine ring, and a Lewis acid promoted formal [3 + 2] cycloaddition/N2 extrusion process to install the polysubstituted cyclopropyl ring.
Process and Intermediates for the Synthesis of 8-[-methyl]-8-phenyl-1,7-diaza-spiro[4.5]decan-2-one Compounds
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Paragraph 0146; 0147, (2014/02/16)
This application discloses a novel process to synthesize 8-[{1-(3,5-Bis-(trifluoromethyl)phenyl)-ethoxy}-methyl]-8-phenyl-1,7-diaza-spiro[4.5]decan-2-one compounds, which may be used, for example, as NK-1 inhibitor compounds in pharmaceutical preparations
