214679-32-0 Usage
Molecular structure
A pyrrolidine ring with a benzyloxy substituent and a succinimide moiety
Usage
Reagent in organic synthesis for the protection of amines
Application
Precursor in the preparation of various pharmaceutical compounds
Chemical properties
Useful in the formation of amide and ester bonds
Modification
Capable of modifying proteins and peptides
Industries
Pharmaceutical research, drug development, and chemical manufacturing
Safety measures
Important to handle and use with proper safety measures due to potential hazards and reactivity
Reactivity
Can react with amines, alcohols, and carboxylic acids to form protected derivatives or esters
Solubility
Soluble in organic solvents such as dichloromethane, tetrahydrofuran, and acetonitrile
Stability
Stable under normal temperature and pressure conditions, but sensitive to moisture and heat
Storage
Should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and heat sources
Hazards
Potential hazards include irritant properties, possible sensitization, and flammability
Disposal
Dispose of in accordance with local, national, and international regulations for hazardous materials
Check Digit Verification of cas no
The CAS Registry Mumber 214679-32-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,6,7 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 214679-32:
(8*2)+(7*1)+(6*4)+(5*6)+(4*7)+(3*9)+(2*3)+(1*2)=140
140 % 10 = 0
So 214679-32-0 is a valid CAS Registry Number.
214679-32-0Relevant academic research and scientific papers
CARBAMATE COMPOUNDS AND OF MAKING AND USING SAME
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Paragraph 00173, (2013/10/08)
Provided herein are carbamate compounds which may be useful in the treatment of, for example, pain, solid tumors and/or obesity.
Asymmetric syntheses of moiramide B and andrimid
Davies, Stephen G.,Dixon, Darren J.
, p. 2635 - 2643 (2007/10/03)
The first highly diastereoselective asymmetric syntheses of moiramide B 2 and andrimid 3 have been achieved using lithium amide (R)-6 and pyrrolidinone auxiliary (R)-9. Pyrrolidinone auxiliary (R)-9 was used to create the novel (S)-3-methyl-N-benzyloxysuc
