24285-39-0 Usage
Description
2-Methylisourea sulfate is a chemical compound that consists of a sulfate group attached to a 2-methylisourea molecule. It is a white crystalline solid that is soluble in water and has a melting point of 210-212°C. This versatile compound is known for its applications in the chemical and pharmaceutical industries.
Used in Pharmaceutical Industry:
2-Methylisourea sulfate is used as an intermediate for the production of pharmaceuticals, playing a crucial role in the synthesis of various medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 2-methylisourea sulfate serves as an intermediate, contributing to the development of products designed to enhance crop protection and yield.
Used as a Reagent in Organic Synthesis:
2-Methylisourea sulfate is utilized as a reagent in organic synthesis, particularly for the formation of heterocyclic compounds, which are essential in creating a wide range of chemical products.
Used in Medical Research:
2-Methylisourea sulfate has been studied for its potential use in the treatment of various medical conditions, including cancer and neurological disorders, highlighting its importance in the ongoing search for new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 24285-39-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,8 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24285-39:
(7*2)+(6*4)+(5*2)+(4*8)+(3*5)+(2*3)+(1*9)=110
110 % 10 = 0
So 24285-39-0 is a valid CAS Registry Number.
InChI:InChI=1/C2H6N2O.H2O4S/c1-5-2(3)4;1-5(2,3)4/h1H3,(H3,3,4);(H2,1,2,3,4)
24285-39-0Relevant articles and documents
O-methyl-isourea carboxylic acid methyl ester preparation
-
Paragraph 0034-0035, (2017/01/26)
The invention discloses a method for preparing O-methyl isourea methyl formate. According to the method, O-methyl isourea bisulfate and methyl chloroformate are put in the mixed solvent of chloroform-water or toluene-water and the like, and O-methyl isourea methyl formate is prepared under alkaline conditions. The method has no step of synthesizing O-methyl isourea sulfate, the production period is shortened, the energy consumption is reduced, the labor intensity of workers is reduced, and the production capacity is improved; the product cost is reduced and the environmental pollution is reduced due to no use of methanol and sodium hydroxide in the method; the water amount in the mixed solvent is strictly controlled, large water amount results in low yield due to large solubility of the product in water; small water amount results in difficult separation of the product due to poor dissolution of inorganic salts produced by the reaction; and the yield is improved by 1-2 percent.
Process for the preparation of 9-deazaguanine derivatives
-
Page 19, (2010/02/09)
Derivatives of 9-deazaguanine are prepared by reacting an aldehyde or ketone with a dialkylaminomalonate to form the corresponding enamine. The enamine is then reacted with a base to form a cyclic pyrrole. The cyclic pyrrole is reacted with an urea compound or a derivative of carbamimidoic acid to provide a protected guanidino compound. The guanidino is converted to the desired 9-deazaguanine derivative by reacting with trifluoracetic acid or with an alkoxide or hydroxide followed by neutralization with an acid.
