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TCI

CAS 2434-53-9

6-Amino-1-methyluracil TCI A2449

6-Amino-1-methyluracil TCI A2449

Chemical Identity

CAS No.
2434-53-9
PubChem
CID 75520·SID 160871358
Formula
C5H7N3O2
Molecular weight
141.13 g/mol
Purity
>98.0%(HPLC)(T)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
6-amino-1-methylpyrimidine-2,4-dione
SMILES
CN1C(=CC(=O)NC1=O)N
InChIKey
GZLZRPNUDBIQBM-UHFFFAOYSA-N
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6-Amino-1-methyluracil is a chemical compound widely utilized in organic synthesis reactions, particularly in the formation of heterocyclic compounds. This versatile building block plays a crucial role in the development of complex molecular structures within laboratory settings. Its unique chemical properties make it an essential component for researchers working on nucleotide analogs and bioactive compounds. In the field of medicinal chemistry, it serves as a foundational material for the synthesis of pharmaceuticals and biologically active substances.

The compound is valued for its solubility in organic solvents, which simplifies processing and purification steps in laboratory workflows. Its molecular structure enables it to participate effectively in substitution and ring-opening reactions, making it a preferred choice for synthetic chemists. The stability of 6-Amino-1-methyluracil under standard laboratory conditions further enhances its utility in various synthetic pathways. Its availability in solid form also facilitates easy handling and use across different experimental scales.

In Indonesian laboratories, 6-Amino-1-methyluracil is commonly used in organic chemistry research, especially in the study of heterocyclic synthesis and drug development. It is frequently employed in academic and research institutions to explore new chemical structures and biological activities. Its role in advancing chemical innovation makes it a vital component in the toolkit of Indonesian scientists and researchers.

  • Organic synthesis of heterocyclic compounds due to its structural versatility and reactivity in ring-opening and substitution reactions.
  • Development of nucleotide analogs for pharmaceutical and biotechnology applications, leveraging its nucleobase-like structure.
  • Investigation of bioactive molecules in medicinal chemistry, supporting the creation of compounds with therapeutic potential.
  • Purification and processing of complex chemical mixtures through its solubility in organic solvents.
  • Educational and research purposes in Indonesian universities and research centers focusing on chemical structure and function.

Brand TCI
CAS number 2434-53-9
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply specifications
Physical form Solid
Storage Store in a cool, dry place away from moisture and direct sunlight

6-Amino-1-methyluracil should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air. Due to its solid form, it is suitable for storage in glass or plastic containers with tight-fitting lids. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment when necessary. It is important to ensure that storage conditions are consistent and free from contaminants to preserve the material's effectiveness in chemical reactions. Proper labeling of containers is essential for safe handling and identification in the laboratory setting.

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