15795-39-8 Usage
Description
1-METHYL-1H-1,2,4-TRIAZOLE-5-AMINE is a chemical compound with the molecular formula C3H5N3. It is a derivative of triazole, which is a five-membered ring with three nitrogen atoms and two carbon atoms. 1-METHYL-1H-1,2,4-TRIAZOLE-5-AMINE is a basic organic amine, characterized by a nitrogen atom that can accept a proton and act as a base in chemical reactions. It serves as a versatile building block in the synthesis of pharmaceuticals and agrochemicals, and also finds applications in the production of specialty chemicals and as a reagent in organic synthesis. 1-METHYL-1H-1,2,4-TRIAZOLE-5-AMINE is an important intermediate compound with diverse uses in the chemical industry.
Uses
Used in Pharmaceutical Industry:
1-METHYL-1H-1,2,4-TRIAZOLE-5-AMINE is used as a building block for the synthesis of various pharmaceuticals. Its unique structure and basic amine properties make it a valuable component in the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 1-METHYL-1H-1,2,4-TRIAZOLE-5-AMINE is utilized as a key intermediate in the production of agrochemicals. Its incorporation into these compounds can contribute to the development of effective pesticides and other agricultural products.
Used in Specialty Chemicals Production:
1-METHYL-1H-1,2,4-TRIAZOLE-5-AMINE is used in the production of specialty chemicals, where its distinctive chemical properties allow for the creation of unique and highly specialized compounds for various applications.
Used as a Reagent in Organic Synthesis:
1-METHYL-1H-1,2,4-TRIAZOLE-5-AMINE also serves as a reagent in organic synthesis, where its ability to act as a base and participate in various chemical reactions is leveraged to facilitate the synthesis of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 15795-39-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,7,9 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15795-39:
(7*1)+(6*5)+(5*7)+(4*9)+(3*5)+(2*3)+(1*9)=138
138 % 10 = 8
So 15795-39-8 is a valid CAS Registry Number.
InChI:InChI=1/C3H6N4/c1-7-3(4)5-2-6-7/h2H,1H3,(H2,4,5,6)
15795-39-8Relevant articles and documents
Synthesis method of 2-methyl-1, 2, 4-triazole-3-amine
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Paragraph 0007; 0009, (2020/09/16)
The invention relates to a synthesis method of 2-methyl-1, 2, 4-triazole-3-amine, and mainly solves the technical problem that no suitable industrial synthesis method exists at present. The method comprises the following three steps: 1, reacting a compound 1 in a solvent 1, 4-dioxane with added N, N-dimethylformamide dimethyl acetal to obtain a compound 2; 2, reacting the compound 2 with triphenylphosphine and diisopropyl azodicarboxylate in methanol to obtain a compound 3; and 3, reacting the compound 3 with sodium hydroxide in methanol and water to obtain a final compound 4, wherein the reaction formula is described in the specification.
Synthesis of 1-Alkyl-5-amino-1,2,4-triazoles Based on Nucleophilic Substitution and Reduction Reactions
Tolstyakov
, p. 1537 - 1547 (2019/01/04)
A series of 1-alkyl-5-amino-1H-1,2,4-triazoles were synthesized starting from 3,5-dibromo-1H- 1,2,4-triazole by alkylation and subsequent nucleophilic substitution of the 5-bromine atom by azido group, reduction of the latter to amino group, and hydrodebromination.
Development of a scaleable process for the synthesis of a next-generation statin
Hobson, Lindsay A.,Akiti, Otute,Deshmukh, Subodh S.,Harper, Shannon,Katipally, Kishta,Lai, Chiajen J.,Livingston, Robert C.,Lo, Ehrlic,Miller, Michael M.,Ramakrishnan, Srividya,Shen, Lifen,Spink, Jan,Tummala, Srinivas,Wei, Chenkou,Yamamoto, Kana,Young, John,Parsons Jr., Rodney L.
scheme or table, p. 441 - 458 (2011/04/22)
This manuscript details the process research and development of a convergent and safe approach to 1 on a multikilo scale. Specific highlights of the process development efforts will be described, including the development of a dehydrogenation method for d