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5-Pyrimidinol, 2-methoxy(9CI) is a pyrimidine derivative chemical compound with the molecular formula C5H6N2O2. It features a methoxy group attached to the 2-position of the pyrimidinol ring, which contributes to its unique structure and properties. 5-Pyrimidinol, 2-methoxy(9CI) serves as a valuable building block in the development of new compounds with potential biological activity, making it significant in the fields of organic and medicinal chemistry.

91233-70-4

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91233-70-4 Usage

Uses

Used in Pharmaceutical Synthesis:
5-Pyrimidinol, 2-methoxy(9CI) is used as a key intermediate in the synthesis of pharmaceuticals for its potential to contribute to the development of new drugs with important industrial and medical applications. Its unique structure allows for the creation of compounds that may exhibit novel therapeutic effects.
Used in Agrochemical Synthesis:
In the agrochemical industry, 5-Pyrimidinol, 2-methoxy(9CI) is utilized as a precursor in the synthesis of agrochemicals, potentially leading to the discovery of new pesticides or other agricultural chemicals that can improve crop protection and yield.
Used in Organic Chemistry Research:
5-Pyrimidinol, 2-methoxy(9CI) is employed as a research compound in organic chemistry, where its properties and reactivity are studied to understand its behavior in various chemical reactions. This research can provide insights into the development of new synthetic methods or the creation of novel organic compounds.
Used in Medicinal Chemistry:
In medicinal chemistry, 5-Pyrimidinol, 2-methoxy(9CI) is used for the exploration of its potential biological activity. Its structure may offer new avenues for the design of compounds that interact with biological targets, possibly leading to the discovery of new therapeutic agents.
Overall, 5-Pyrimidinol, 2-methoxy(9CI) is a versatile compound with applications across multiple industries, primarily due to its role in the synthesis of pharmaceuticals and agrochemicals, and its potential in organic and medicinal chemistry research. Further exploration of 5-Pyrimidinol, 2-methoxy- (9CI) could unlock new possibilities in drug discovery and chemical innovation.

Check Digit Verification of cas no

The CAS Registry Mumber 91233-70-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,2,3 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 91233-70:
(7*9)+(6*1)+(5*2)+(4*3)+(3*3)+(2*7)+(1*0)=114
114 % 10 = 4
So 91233-70-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H6N2O2/c1-9-5-6-2-4(8)3-7-5/h2-3,8H,1H3

91233-70-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methoxypyrimidin-5-ol

1.2 Other means of identification

Product number -
Other names 5-HYDROXY-2-METHOXYPYRIMIDINE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:91233-70-4 SDS

91233-70-4Downstream Products

91233-70-4Relevant academic research and scientific papers

C70 Fullerene-Catalyzed Metal-Free Photocatalytic ipso-Hydroxylation of Aryl Boronic Acids: Synthesis of Phenols

Kumar, Inder,Sharma, Ritika,Kumar, Rakesh,Kumar, Rakesh,Sharma, Upendra

supporting information, p. 2013 - 2019 (2018/04/02)

A metal-free C70 fullerene-catalyzed method has been developed for the ipso-hydroxylation of aryl and heteroaryl boronic acids to corresponding phenols under photocatalytic conditions. The reaction proceeds under oxygen atmosphere and the mechanistic study revealed that C70 plays a critical role in the generation of reactive oxygen species in the presence of blue light. Reactions in the presence of 18O-labelled water and oxygen confirmed the generation of reactive oxygen species from oxygen molecule. Amine used as a reductant could be recovered in the form of imine. The current method is also applicable to the synthesis of aryl ethers in one-pot two-step process. (Figure presented.).

Synthesis of some pyrimidine N-oxides

Jovanovic, Misa V.

, p. 1176 - 1180 (2007/10/02)

Various monosubstitudes pyrimidines and methylpyrimidines were N-oxidized with a number of different peracids.In general, they are more susceptible to side reactions accompanying N-oxidation (i.e., decomposition, annular carbon oxidation, ring opening) than other ?-deficient diazine and triazine analogs.Unsymmetrical pyrimidines, which can potentially yield two isomeric products, were N-oxidized preferentially at the site para to strong electron-donating substituents.Weaker ringactivating groups, such as methyl, are mainly ortho directing and only aid in the N-oxidation of pyrimidine nuclei having ortho/para-directing substituents.

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