70631-93-5 Usage
Uses
Used in Pharmaceutical Synthesis:
4-METHYL-1H-IMIDAZOLE-2-CARBOXYLICACID is used as a key intermediate in the synthesis of pharmaceuticals for its ability to form essential components of various drug molecules, contributing to the development of new medications.
Used in Agrochemical Production:
In the agrochemical industry, 4-METHYL-1H-IMIDAZOLE-2-CARBOXYLICACID is utilized as a building block for the creation of active ingredients in pesticides and other agricultural chemicals, enhancing crop protection and yield.
Used in Dye and Pigment Manufacturing:
4-METHYL-1H-IMIDAZOLE-2-CARBOXYLICACID is used as a chemical component in the manufacturing of dyes and pigments, providing a range of colors and properties for various applications in industries such as textiles, plastics, and inks.
Used in Materials Science:
Within the field of materials science, 4-METHYL-1H-IMIDAZOLE-2-CARBOXYLICACID has potential applications in the development of new materials, possibly due to its ability to form complexes or participate in specific chemical reactions that enhance material properties.
Used as a Research Tool in Chemical Biology:
4-METHYL-1H-IMIDAZOLE-2-CARBOXYLICACID also serves as a valuable research tool in chemical biology, where it can be employed to study biological processes or to develop new chemical probes for investigating molecular interactions.
Check Digit Verification of cas no
The CAS Registry Mumber 70631-93-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,3 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 70631-93:
(7*7)+(6*0)+(5*6)+(4*3)+(3*1)+(2*9)+(1*3)=115
115 % 10 = 5
So 70631-93-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H6N2O2/c1-3-2-6-4(7-3)5(8)9/h2H,1H3,(H,6,7)(H,8,9)
70631-93-5Relevant academic research and scientific papers
Synthesis of 4-Methylimidazole-2-Carboxylic Acid
Wang, Xianheng,Zhao, Changkuo,Gao, Lei,Zhou, Yiqi,Xu, Lang
, p. 2619 - 2622 (2018/09/25)
4-Methylimidazole-2-carboxylic acid was synthesized from 4-methylimidazole with a total yield of 65% over four steps including an N-benzyl protection, acylation, debenzylation, and ester hydrolysis. The solvent, base, temperature, and reaction time are op
4-alkyl-imidazole-2-carboxylic acid synthesizing method
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Paragraph 0028-0030; 0038; 0039, (2017/01/26)
The invention provides a method for synthesizing 4-alkylimidazole-2-carboxylic acid I. The method comprises the steps of firstly, reacting 2-alkyl-imidazole II as a raw material with BnX in the presence of a base to generate a mixture of a pair of position isomers IIIa and IIIb; secondly, on the premise that the mixture is not separated, reacting the mixture with halogenated formate (i.e., XCOOR2) in the presence of a base to generate a pair of corresponding isomers IVa and IVb; thirdly, hydrogenating to remove a benzyl group V in the presence of a hydrogenation catalyst; and fourthly, in the presence of a base, hydrolyzing to obtain the desired product 4-alkylimidazole-2-carboxylic acid I. The reaction route is shown in the specification, wherein R1 is selected from hydrogen atom and lower alkyl groups such as methyl and ethyl and R2 is selected from C1-C6 alkyl, C1-C6 alkoxy substituted group, a phenyl group or a benzyl group. The method disclosed by the invention has ingenious concept, since an inexpensive reagent is used in the respective step, and the yield of each step is high, the final target product 4-alkylimidazole-2-carboxylic acid I can be obtained in efficiency, convenience and low cost.
