3117-61-1 Usage
Description
N-Salicylideneamine, also known as salicylaldimine, is an organic compound belonging to the class of salicylaldehyde imines. It is characterized by a phenol group with an iminomethyl substituent at the 2-position. N-Salicylideneamine has attracted interest due to its potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
N-Salicylideneamine is used as a building block for the synthesis of various pharmaceutical compounds. Its unique structure allows for the creation of a wide range of molecules with different biological activities, making it a valuable asset in drug discovery and development.
Used in Chemical Synthesis:
N-Salicylideneamine serves as an important intermediate in the synthesis of various organic compounds, including dyes, pigments, and other specialty chemicals. Its reactivity and versatility make it a popular choice for researchers and chemists working in the field of organic synthesis.
Used in Material Science:
Due to its structural properties, N-Salicylideneamine can be utilized in the development of new materials with specific properties, such as conductivity, magnetism, or optical characteristics. It can be incorporated into polymers, nanoparticles, or other advanced materials to enhance their performance and functionality.
Used in Analytical Chemistry:
N-Salicylideneamine can be employed as a reagent or a colorimetric indicator in various analytical techniques. Its ability to form complexes with different metal ions makes it useful for the detection and quantification of specific elements in chemical analysis.
Check Digit Verification of cas no
The CAS Registry Mumber 3117-61-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,1 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3117-61:
(6*3)+(5*1)+(4*1)+(3*7)+(2*6)+(1*1)=61
61 % 10 = 1
So 3117-61-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NO/c8-5-6-3-1-2-4-7(6)9/h1-5H,8H2/b6-5-
3117-61-1Relevant articles and documents
Variability of the Transformations of 4-Hydroxy-6-methyl-2H-pyran-2-one under Modified Biginelli Reaction Conditions
Strashilina,Mazhukina,Fedotova
, p. 102 - 106 (2018/06/14)
A modified version of the three-component Biginelli reaction of 4-hydroxy-6-methyl-2H-pyran-2-one with aromatic aldehydes in urea under conventional heating and microwave activation has been studied. Depending on the order of addition of the reactants, su
Time-resolved E.S.R. Study of Triplet Ketoamines Generated by Intramolecular Proton Transfer in Free Schiff Bases
Tero-Kubota, Shozo,Migita, Kouto,Akiyama, Kimio,Ikegami, Yusaku
, p. 1067 - 1068 (2007/10/02)
Non-phosphorescent triplet states of the ketoamine forms of several free Schiff bases generated by intramolecular proton transfer have been observed using a time-resolved e.s.r. method.