933751-05-4 Usage
Description
5-Thiazolemethanamine, N-methyl-, also known as 5-Methylthiazolamine, is a chemical compound with the molecular formula C4H6N2S. It is a derivative of thiazole and exists as a colorless to light yellow liquid at room temperature. 5-Thiazolemethanamine, N-methylis recognized for its unique reactivity and biological activity due to the presence of the thiazole ring, making it a valuable building block in organic synthesis.
Used in Pharmaceutical Industry:
5-Thiazolemethanamine, N-methylis utilized as an intermediate in the synthesis of pharmaceuticals. Its unique structure and properties allow it to be a key component in the development of various medications, contributing to the creation of new and effective drugs.
Used in Agrochemical Industry:
In the agrochemical sector, 5-Thiazolemethanamine, N-methylserves as an intermediate in the production of agrochemicals. Its application aids in the synthesis of compounds that are beneficial for agricultural purposes, such as pesticides and herbicides, enhancing crop protection and yield.
Used in Material Science:
5-Thiazolemethanamine, N-methylhas potential applications in the development of new materials and chemicals. Its unique properties can be harnessed to create innovative materials with specific characteristics, useful in various industries.
However, it is crucial to handle 5-Thiazolemethanamine, N-methylwith care, as it may present certain hazards and risks to human health and the environment. Proper safety measures and precautions should be taken during its production, use, and disposal to mitigate any potential adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 933751-05-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,3,7,5 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 933751-05:
(8*9)+(7*3)+(6*3)+(5*7)+(4*5)+(3*1)+(2*0)+(1*5)=174
174 % 10 = 4
So 933751-05-4 is a valid CAS Registry Number.
933751-05-4Relevant articles and documents
Thiazole alkyl pyridylamine compound and preparation method and application thereof
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Paragraph 0075; 0076; 0078, (2016/10/09)
The present invention discloses a thiazole alkyl pyridylamine compound shown in formula (I) and a preparation method and application thereof, wherein R, R ', Z, R1 and R2 are as defined in the specification. The thiazole alkyl pyridylamine compound shown in formula (I) has bactericidal, acaricidal or herbicidal biologically activity, and has high activity on pathogenic bacteria such as sclerotinia sclerotiorum, botrytis cinerea pers, and the like.
Discovery of novel thieno[2,3-d]pyrimidin-4-yl hydrazone-based cyclin-dependent kinase 4 inhibitors: synthesis, biological evaluation and structure-activity relationships
Horiuchi, Takao,Takeda, Yasuyuki,Haginoya, Noriyasu,Miyazaki, Masaki,Nagata, Motoko,Kitagawa, Mayumi,Akahane, Kouichi,Uoto, Kouichi
experimental part, p. 991 - 1002 (2011/10/02)
The design, synthesis, and evaluation of novel thieno[2,3-d]pyrimidin-4-yl hydrazone analogues as cyclin-dependent kinase 4 (CDK4) inhibitors are described. In continuing our program aim to search for potent CDK4 inhibitors, the introduction of a thiazole group at the hydrazone part has led to marked enhancement of chemical stability. Furthermore, by focusing on the optimization at the C-4′ position of the thiazole ring and the C-6 position of the thieno[2,3-d]pyrimidine moiety, compound 35 has been identified with efficacy in a xenograft model of HCT116 cells. In this paper, the potency, selectivity profile, and structure-activity relationships of our synthetic compounds are discussed.
