2735-61-7 Usage
Uses
Used in Pharmaceutical Research and Development:
(1-Methyl-1H-benzoimidazol-2-yl)-acetic acid ethyl ester is used as a research compound for exploring its potential pharmacological properties. Its unique structure may contribute to various therapeutic applications, such as the development of new drugs or drug candidates.
Used in Chemical Synthesis:
(1-Methyl-1H-benzoimidazol-2-yl)-acetic acid ethyl ester may also be used as an intermediate in the synthesis of other related chemical compounds, particularly those belonging to the benzoimidazole class. Its versatility in chemical reactions can facilitate the creation of new molecules with potential applications in various fields.
Used in Material Science:
Due to its structural features, (1-Methyl-1H-benzoimidazol-2-yl)-acetic acid ethyl ester may have potential applications in material science, such as the development of new materials with specific properties or the modification of existing materials to enhance their performance.
Check Digit Verification of cas no
The CAS Registry Mumber 2735-61-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,3 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2735-61:
(6*2)+(5*7)+(4*3)+(3*5)+(2*6)+(1*1)=87
87 % 10 = 7
So 2735-61-7 is a valid CAS Registry Number.
2735-61-7Relevant academic research and scientific papers
Synthesis and photochromic properties of 2-(3-nitro-2-pyridylmethyl)benzazoles
Zakhs,Ponyaev,Subbotina,El'tsov
, p. 1076 - 1087 (2007/10/03)
2-(3-Nitro-2-pyridylmethyl)benzazoles were synthesized, and their photochromic properties were studied by flash photolysis. Introduction of a nitropyridyl instead of the nitrophenyl moiety into the 2-methyl group insignificantly increases the basicity of the methylene group. Nitropyridyl-substituted benzazoles give rise to three detectable photoinduced forms: the corresponding union at pH > 10, azamerocyanine at pH ≈ 4, and monomethinecyanine at pH ≈ 1. Irradiation of solutions of weakly basic henzoxazole and benzothiazole derivatives at pH ≈ 4 results in formation of neutral chelate structures in which the hydrogen atom is linked simultaneously to two nitrogen atoms: one in the pyridine ring, and the second, in the azole ring.
Conversion of some azaheterocyclic-acetic esters and -acetonitriles into fused heterocycles
McKinnon, David M.,Spevack, Perry,Tipples, Graham
, p. 2339 - 2344 (2007/10/02)
Various heterocyclic acid esters and nitriles of the pyridine, thiazole, and imidazole series react with 3-methylthio-4-phenyl-1,2-dithiolium perchlorate to form fused pyridinethiones or dithiolylidene esters.These esters or nitriles also react with trichloromethanesulfenyl chloride to form fused isothiazoles.
