85725-66-2 Usage
Chemical Type
Ester derivative of azetidinecarboxylic acid
Application
Pharmaceutical Industry: Widely used in pharmaceutical industry.
Synthesis: Used as a building block in the synthesis of various drugs and pharmaceutical compounds.
Research and Development: Utilized in research and development for drug discovery.
Organic Synthesis: Serves as a reagent in organic synthesis.
Properties
Potential: Has potential as a building block in drug synthesis.
Versatile: Can be used in the synthesis of bioactive molecules.
Wide Range of Applications: Used in drug manufacturing processes.
Usage
Drug Synthesis: Used as a precursor in the synthesis of drugs.
Bioactive Molecules: Used in the synthesis of various bioactive molecules.
Research: Employed in research and development.
Reagent
Utilized as a reagent in organic synthesis and drug manufacturing.
Importance
Pharmaceutical Industry: Significant importance in pharmaceutical applications.
Drug Discovery: Contributes to drug discovery efforts.
Synthetic Chemistry: Valuable in synthetic chemistry processes.
Specific Content
Chemical Structure:
Consists of an azetidinecarboxylic acid core.
Contains an ethyl ester group.
Contains a 2,4-dimethoxyphenylmethyl group.
Features an ethylidene and oxo group.
Functionality:
Plays a crucial role as a building block.
Acts as a precursor in drug synthesis.
Used in the production of bioactive compounds.
Application in Drug Manufacturing:
Key component in drug manufacturing processes.
Enables the synthesis of pharmaceuticals.
Utility in Research:
Facilitates research in drug development.
Used in laboratory settings for experimentation.
Potential Benefits
Efficiency: Enhances efficiency in drug synthesis.
Diversity: Allows for the creation of diverse pharmaceutical compounds.
Versatility: Offers versatility in drug design and synthesis.
Safety Considerations
Safety data and precautions may vary based on specific applications and handling procedures.
Check Digit Verification of cas no
The CAS Registry Mumber 85725-66-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,7,2 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 85725-66:
(7*8)+(6*5)+(5*7)+(4*2)+(3*5)+(2*6)+(1*6)=162
162 % 10 = 2
So 85725-66-2 is a valid CAS Registry Number.
85725-66-2Relevant academic research and scientific papers
Base-induced Cyclization of N--2-bromo-3-hydroxybutyramide Derivatives
Shiozaki, Masao,Ishida, Noboru,Hiraoka, Tetsuo,Maruyama, Hiroshi
, p. 2135 - 2139 (2007/10/02)
Treatment of (2R,3R)-N-(2,4-dimethoxybenzyl)-N--2-bromo-3-hydroxybutyramide (5) with DBU yielded the bicyclic β-lactam 13 by a direct cyclization, and its diastereoisomer 14 and the γ-lactam 15 via the trans-epoxide 6.The same t
BASE-INDUCED CYCLIZATION OF (2R,3R)- AND (2S,3R)-N-2,4-DIMETHOXYBENZYL-N-BIS(ETHOXYCARBONYL)METHYL-2-BROMO-3-HYDROXYBUTYLAMIDE
Shiozaki, Masao,Ishida, Noboru,Hiraoka, Tetsuo,Maruyama, Hiroshi
, p. 169 - 172 (2007/10/02)
Reaction of (2R,3R)-N-2,4-dimethoxybenzyl-N-bis(ethoxycarbonyl)methyl-2-bromo-3-hydroxybutylamide (6) with DBU yielded bicyclic β-lactam 7 by a direct cyclization, and its diastereomer 8 and unexpected γ-lactam 9 by another non-direct cyclization.Also (2S
