54149-64-3 Usage
Uses
Used in Organic Synthesis:
O-(2-Methyl-allyl)-hydroxylamine hydrochloride serves as a reagent in organic synthesis, particularly for the preparation of oximes. These oximes are crucial intermediates in the synthesis of a broad spectrum of pharmaceuticals and agrochemicals, highlighting the compound's importance in the development of new and existing products within these industries.
Used in Chemical Research:
As a component in chemical research, O-(2-Methyl-allyl)-hydroxylamine hydrochloride aids in the exploration and understanding of chemical reactions and mechanisms. Its unique structure allows researchers to investigate a variety of chemical pathways and interactions, contributing to the advancement of scientific knowledge.
Used in the Production of Rubber Chemicals:
O-(2-Methyl-allyl)-hydroxylamine hydrochloride acts as a precursor in the manufacturing process of rubber chemicals. Its role in this industry is vital for the creation of additives and other compounds that enhance the performance and properties of rubber products.
Used in the Production of Fuel Additives:
O-(2-Methyl-allyl)-hydroxylamine hydrochloride also finds application in the production of fuel additives. Its inclusion in fuel formulations can contribute to improved fuel performance, efficiency, and potentially reduce harmful emissions.
Used in Pharmaceutical Industry:
O-(2-Methyl-allyl)-hydroxylamine hydrochloride is utilized in the pharmaceutical sector as a starting material for the synthesis of various drugs. Its versatility and reactivity make it a valuable component in the development of new medications and therapies.
Overall, O-(2-Methyl-allyl)-hydroxylamine hydrochloride is a multifaceted chemical with a diverse range of applications across different industries, including organic synthesis, chemical research, rubber and fuel additive production, and pharmaceutical development. Its water solubility as a hydrochloride salt further enhances its utility in aqueous reactions and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 54149-64-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,4 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54149-64:
(7*5)+(6*4)+(5*1)+(4*4)+(3*9)+(2*6)+(1*4)=123
123 % 10 = 3
So 54149-64-3 is a valid CAS Registry Number.
54149-64-3Relevant academic research and scientific papers
Synthesis of oxazinyl analogues of fosmidomycin using RCM methodology
Van Der Jeught, Sarah,Stevens, Christian V.,Dieltiens, Nicolai
, p. 3183 - 3187 (2008/09/19)
Fosmidomycin is a promising antimalarial compound with a novel mode of action, the inhibition of 1-deoxy-D-xylulose 5-phosphate reductoisomerase, a key enzyme in the biosynthesis of isoprenoids through the nonmevalonate pathway. This paper describes the synthesis of a series of analogues in which the hydroxamate moiety is incorporated in a ring structure, leaving the complexation with the enzyme up to the oxygen lone pairs instead of the free hydroxyl group. The antimalarial activities of the different analogues are currently under investigation. Georg Thieme Verlag Stuttgart.
