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5-(Hydroxymethyl)-2-methylpyrimidin-4-ol is a pyrimidine derivative with a molecular formula C6H8N2O2. It features a hydroxymethyl group at the 5th position and a methyl group at the 2nd position on the pyrimidine ring. This chemical compound is recognized for its role as a precursor in the synthesis of nucleoside analogs, which are of interest in pharmaceuticals and antiviral drug development. Its potential biological activity is currently under investigation, with ongoing research aimed at uncovering its possible therapeutic properties. Furthermore, it serves as a crucial intermediate in the synthesis of various organic compounds, highlighting its value in the chemical and pharmaceutical industries.

698-30-6

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698-30-6 Usage

Uses

Used in Pharmaceutical Industry:
5-(Hydroxymethyl)-2-methylpyrimidin-4-ol is used as a precursor in the synthesis of nucleoside analogs for their potential applications in pharmaceuticals and antiviral drugs. Its unique structure allows for the development of compounds that can target specific viral processes, offering new avenues for treatment.
Used in Chemical Industry:
As an important intermediate, 5-(Hydroxymethyl)-2-methylpyrimidin-4-ol is utilized in the synthesis of other organic compounds. Its presence in various chemical reactions contributes to the creation of a wide range of products, underlining its versatility and importance in chemical synthesis processes.
Used in Antiviral Drug Development:
5-(Hydroxymethyl)-2-methylpyrimidin-4-ol is employed as a key component in the development of antiviral drugs. Its role in the synthesis of nucleoside analogs makes it instrumental in creating medications that can inhibit viral replication and reduce the severity of viral infections.
Used in Research and Development:
5-(HYDROXYMETHYL)-2-METHYLPYRIMIDIN-4-OL is used as a subject of research to explore its biological activity and potential therapeutic properties. Ongoing studies aim to understand its interactions with biological systems and its efficacy in treating various conditions, which could lead to new therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 698-30-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 698-30:
(5*6)+(4*9)+(3*8)+(2*3)+(1*0)=96
96 % 10 = 6
So 698-30-6 is a valid CAS Registry Number.

698-30-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(hydroxymethyl)-2-methyl-1H-pyrimidin-6-one

1.2 Other means of identification

Product number -
Other names 5-hydroxymethyl-2-methyl-3H-pyrimidin-4-one

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:698-30-6 SDS

698-30-6Relevant academic research and scientific papers

Thiamine Biosynthesis in Yeast - Evaluation of 4-Hydroxy-5-hydroxymethyl-2-methylpyrimidine as a Precursor

Baxter, Robert L.,Hanley, A. Bryan,Chan, Henry W. S.

, p. 2963 - 2966 (2007/10/02)

The putative role of 4-hydroxy-5-hydroxymethyl-2-methylpyrimidine 2 as a late precursor in the biosynthesis of thiamine 1 by Saccharomyces cerevisiae has been examined using the deuteriated derivative 2a.To enable measurement of deuterium incorporation into the pyrimidine ring fragment of 1, a procedure for the degradation of 1 to the aniline derivative 6 using thiaminase I from Bacillus thiaminolyticus has been developed.While 4-amino-2-methyl-5-hydroxymethylpyrimidine 3a was incorporated into thiamine, deuterium from hydroxy-pyrimidine 2a was not incorporated to any significant extent, indicating that amination of compound 2 is not a late step in the biosynthesis of the pyrimidine ring.

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