397886-88-3 Usage
Uses
Used in Pharmaceutical Industry:
1-Oxa-5-azaspiro[5.5]undec-2-ene-2-carboxylic acid, 5-(2-bromo-1-oxopropyl)-4-oxo-3-phenyl-, methyl ester is used as a potential drug candidate for the development of new medications. Its unique structure and functional groups can be utilized to target specific biological pathways or receptors, leading to the discovery of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, 1-Oxa-5-azaspiro[5.5]undec-2-ene-2-carboxylic acid, 5-(2-bromo-1-oxopropyl)-4-oxo-3-phenyl-, methyl ester can be employed as a potential active ingredient in the development of new pesticides or herbicides. Its unique structure and functional groups may provide novel modes of action or improved efficacy against pests and weeds.
Used in Materials Science:
1-Oxa-5-azaspiro[5.5]undec-2-ene-2-carboxylic acid, 5-(2-bromo-1-oxopropyl)-4-oxo-3-phenyl-, methyl ester can be used as a building block or component in the development of new materials with specific properties. Its unique structure and functional groups may contribute to the creation of advanced materials for various applications, such as sensors, catalysts, or advanced polymers.
Check Digit Verification of cas no
The CAS Registry Mumber 397886-88-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,7,8,8 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 397886-88:
(8*3)+(7*9)+(6*7)+(5*8)+(4*8)+(3*6)+(2*8)+(1*8)=243
243 % 10 = 3
So 397886-88-3 is a valid CAS Registry Number.
397886-88-3Relevant academic research and scientific papers
2,3-Dihydro-4H-1,3-oxazin-4-ones, novel auxiliaries for the stereoselective synthesis of 1β-methylcarbapenems
Pyun,Jeong,Jung,Kim,Lee,Lee,Kim
, p. 1950 - 1952 (2007/10/03)
Dihydrooxazinones 9, prepared from benzylcyanide in two steps serve as efficient auxiliaries for the stereoselective synthesis of β-methylcarbapenem intermediate 2. Reformatsky-type reactions of 4-acetoxyazetidinone with α-bromopropionyl dihydrooxazinone 10 provided β-methylazetidinones 4 in high diastereoselectivities. The auxiliaries 9 were also easily removed in the Dieckmann cyclization leading to β-methylcarbapenem skeletons. Practical synthesis of β-methylenolphosphates 2 from 4-acetoxyazetidinone 3 was achieved in three steps (61-77% overall yield).
