CAS 3289-47-2

2-O-Methylcytosine

Description:

2-O-Methylcytosine is a modified nucleoside derived from cytosine, characterized by the addition of a methoxy group at the 2-position of the pyrimidine ring. This modification can influence the stability and reactivity of nucleic acids, affecting processes such as transcription and translation. The presence of the methoxy group can enhance the hydrophobicity of the molecule, potentially impacting its interactions with proteins and other biomolecules. 2-O-Methylcytosine is often found in various biological contexts, particularly in RNA, where it plays a role in the regulation of gene expression and the modulation of RNA structure. Its presence can also be indicative of specific cellular processes or conditions, making it a subject of interest in molecular biology and biochemistry. The compound is typically studied in the context of epigenetics and RNA biology, where modifications to nucleotides can have significant implications for cellular function and gene regulation.

Formula: C₅H₇N₃O

InChI: InChI=1S/C5H7N3O/c1-9-5-7-3-2-4(6)8-5/h2-3H,1H3,(H2,6,7,8)

InChI key: InChIKey=DHYLZDVDOQLEAQ-UHFFFAOYSA-N

SMILES: O(C)C=1N=C(N)C=CN1

Synonyms:

• 2-Methoxycytosine
• 2-Methoxypyrimidin-4-Amine
• 2-O-Methylcytosine
• 4-Amino-2-methoxypyrimidine
• 4-Pyrimidinamine, 2-Methoxy-
• Pyrimidine, 4-amino-2-methoxy-
• 2-Methoxy-4-pyrimidinamine

4-Pyrimidinamine, 2-methoxy- (9CI)

CAS: 3289-47-2

Formula: C₅H₇N₃O

Purity: 95%

Color and Shape: Solid

Molecular weight: 125.1286

Ref: IN-DA00C7LF

4-Amino-2-methoxypyrimidine

CAS: 3289-47-2

4-Amino-2-methoxypyrimidine

Formula: C₅H₇N₃O

Purity: 97%

Color and Shape: white to off white solid

Molecular weight: 125.13g/mol

Ref: 54-OR16620

4-Amino-2-methoxypyrimidine

CAS: 3289-47-2

Formula: C₅H₇N₃O

Purity: 97%

Color and Shape: Solid

Molecular weight: 125.131

Ref: 10-F079937

4-Amino-2-methoxypyrimidine

CAS: 3289-47-2

4-Amino-2-methoxypyrimidine is a fluorescent compound that is used for the detection of hydrogen bonds, and as a precursor in the synthesis of other compounds. 4-Amino-2-methoxypyrimidine has been shown to be able to absorb ultraviolet radiation, which leads to its fluorescence. The compound can also form hydrogen bonds with other molecules and it has been shown to react with n-hexane. 4-Amino-2-methoxypyrimidine reacts with orthophosphate, producing singlet oxygen and transferring a proton. It also reacts with solvents such as water or ethanol, giving off light.

Formula: C₅H₇N₃O

Purity: Min. 95%

Molecular weight: 125.13 g/mol

Ref: 3D-NA57396