69079-09-0 Usage
Uses
Used in Pharmaceutical Industry:
3-oxo-1-Pyrrolidinecarboxylic acid Methyl ester is used as an intermediate for the synthesis of various pharmaceuticals. Its role in the production of drugs is crucial, as it aids in the development of new medications and the improvement of existing ones.
Used in Agricultural Chemicals Industry:
In the agricultural chemicals sector, 3-oxo-1-Pyrrolidinecarboxylic acid Methyl ester is utilized as an intermediate in the production of agrochemicals. This involvement helps in creating effective solutions for pest control and crop protection, contributing to increased agricultural productivity.
Used as a Reagent in Organic Synthesis:
3-oxo-1-Pyrrolidinecarboxylic acid Methyl ester also serves as a reagent in organic synthesis, enabling chemists to carry out a range of chemical reactions. Its versatility in this context is valuable for the development of new chemical compounds and materials.
Safety Precautions:
Check Digit Verification of cas no
The CAS Registry Mumber 69079-09-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,0,7 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69079-09:
(7*6)+(6*9)+(5*0)+(4*7)+(3*9)+(2*0)+(1*9)=160
160 % 10 = 0
So 69079-09-0 is a valid CAS Registry Number.
69079-09-0Relevant articles and documents
An improved synthesis of methyl 1,3-dihydro-2H-pyrrolo[3,4-b]quinoline-2- carboxylate
Akue-Gedu, Rufine,Gautret, Philippe,Lelieur, Jean-Pierre,Rigo, Benoit
, p. 3319 - 3322 (2008/09/20)
Optimization of an old route leads very easily, in four steps, to methyl 1,3-dihydro-2H-pyrrolo[3,4-b]quinoline-2-carboxylate in 45% yield from commercial starting materials. This procedure can be compared to recently described methods whose yields were o
A convenient method for introducing oxo group into the β-position of cyclic amines and its application to synthesis of δ-aminolevulinic acid
Matsumura,Takeshima,Okita
, p. 304 - 306 (2007/10/02)
Oxo group could be introduced into the β-position of N-methoxycarbonylated cyclic amines by utilizing electrochemical oxidation and/or m-chloroperbenzoic acid oxidation, and this method was applied to the preparation of δ-aminolevulinic acid, an intermediate of chlorophyll biosynthesis.
Preparation of 3-pyrrolidone and 4-perhydroazepinone
Roglans,Marquet,Moreno-Manas
, p. 1249 - 1258 (2007/10/02)
Efficient multigram preparations of 3-pyrrolidone by sequential Michael addition and Dieckmann condensation, and of 4-perhydroazepinone by ring expansion have been achieved.
