36342-07-1 Usage
Description
N-N-PROPYLMALEAMIC ACID, 98 is an organic compound that serves as a valuable research reagent in the field of organic synthesis and various chemical processes. It is known for its unique chemical properties that make it suitable for a wide range of applications.
Uses
Used in Research and Development:
N-N-PROPYLMALEAMIC ACID, 98 is used as a research reagent for organic synthesis and other chemical processes. Its unique chemical properties make it a valuable tool for scientists and researchers in the development of new compounds and materials.
Used in Pharmaceutical Industry:
N-N-PROPYLMALEAMIC ACID, 98 is used as an intermediate in the synthesis of various pharmaceutical compounds. Its versatility in chemical reactions allows for the creation of a wide range of drug candidates with potential therapeutic applications.
Used in Chemical Synthesis:
N-N-PROPYLMALEAMIC ACID, 98 is used as a building block in the synthesis of various organic compounds. Its reactivity and functional groups make it a useful component in the development of new molecules with specific properties and applications.
Used in Material Science:
N-N-PROPYLMALEAMIC ACID, 98 can be used as a component in the development of new materials with unique properties. Its chemical structure allows for the creation of materials with specific characteristics, such as improved strength, flexibility, or chemical resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 36342-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,3,4 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 36342-07:
(7*3)+(6*6)+(5*3)+(4*4)+(3*2)+(2*0)+(1*7)=101
101 % 10 = 1
So 36342-07-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H11NO3/c1-2-5-8-6(9)3-4-7(10)11/h3-4H,2,5H2,1H3,(H,8,9)(H,10,11)/b4-3+
36342-07-1Relevant articles and documents
Synthesis and antimicrobial activities of N-substituted imides
Zentz, Frederic,Valla, Alain,Le Guillou, Regis,Labia, Roger,Mathot, Anne-Gabrielle,Sirot, Danielle
, p. 421 - 426 (2007/10/03)
In the field of our research programs concerning novel antimicrobial agents, a series of N-substituted imides was synthesized. These compounds were obtained by cyclization of amido-acids in acetic anhydride/sodium acetate or hexamethyldisilazane/zinc bromide for the hydroxy-aromatic derivatives. The hydroxy-alkyl maleimides were directly prepared by condensation of the corresponding amino-alcohol with maleic anhydride in boiling toluene. Most of N-substituted maleimides showed an interesting antimicrobial activity towards bacteria from the ATCC collection (Staphylococcus aureus ATCC 25923, Enterococcus faecalis ATCC 29212, Escherichia coli ATCC 25922 and Pseudomonas aeruginosa ATCC 27853) but the MIC values for P. aeruginosa were always high (128 μg/ml). The imides with alkyl substituents showed higher activities than aromatic analogues with MIC values in the range of 8-32 μg/ml. Comparatively, succinimides were practically inactive.