Skip to main content

Pyridoxal

ADVERTISEMENT
Identification
Molecular formula
C6H9N3O
CAS number
65-22-5
IUPAC name
(4-amino-2-methyl-pyrimidin-5-yl)methanol
State
State

The compound is a solid at room temperature.

Melting point (Celsius)
166.00
Melting point (Kelvin)
439.15
Boiling point (Celsius)
295.00
Boiling point (Kelvin)
568.15
General information
Molecular weight
124.15g/mol
Molar mass
124.1470g/mol
Density
1.2580g/cm3
Appearence

The compound appears as a white to off-white powder or solid.

Comment on solubility

Solubility of (4-amino-2-methyl-pyrimidin-5-yl)methanol

The solubility of the compound (4-amino-2-methyl-pyrimidin-5-yl)methanol (C6H9N3O) can be influenced by various factors. Generally, its solubility can be described as follows:

  • Polar Characteristics: Due to the presence of the -OH group, this compound exhibits polar characteristics, which may enhance its solubility in polar solvents such as water.
  • Hydrogen Bonding: The ability to form hydrogen bonds can significantly affect solubility. Compounds with amino and hydroxyl groups can engage in hydrogen bonding with solvent molecules, potentially improving their solubility.
  • Temperature Dependence: As with many organic compounds, solubility may increase with temperature. Therefore, heating the solvent might aid in dissolving this compound more effectively.
  • pH Influence: The degree of ionization of the amino group can be affected by the pH of the solution. In more acidic conditions, the amino group can become protonated, possibly increasing solubility.

Overall, one could expect that (4-amino-2-methyl-pyrimidin-5-yl)methanol's solubility in various solvents will vary based on these factors, making it crucial to consider the environment in which it is utilized. Understanding these solubility traits not only aids in practical applications but also in predicting the behavior of the compound in biological systems.

Interesting facts

Interesting Facts about (4-amino-2-methyl-pyrimidin-5-yl)methanol

(4-amino-2-methyl-pyrimidin-5-yl)methanol, often referred to in the context of pyrimidine derivatives, is a fascinating compound with a variety of noteworthy applications and properties.

Key Insights:

  • Biological Relevance: Pyrimidines play a critical role in biology, particularly as components of nucleotides, which are the building blocks of DNA and RNA. This compound's structure suggests potential interactions with biological systems, making it a candidate for further pharmacological exploration.
  • Synthesis and Versatility: The synthesis of pyrimidine derivatives like this one can be achieved through various methods, including reactions involving amines and aldehydes. This versatility opens doors for the creation of numerous derivatives with tailored properties.
  • Potential Therapeutic Applications: Due to the presence of amino and hydroxymethyl groups, compounds like (4-amino-2-methyl-pyrimidin-5-yl)methanol may exhibit biological activity. Researchers are interested in their potential as anti-cancer, anti-viral, or anti-inflammatory agents.
  • Importance in Drug Design: The unique combination of functional groups in this compound can be pivotal in the field of medicinal chemistry. Understanding how variations in the structure influence biological activity is crucial for drug development.

In summary, (4-amino-2-methyl-pyrimidin-5-yl)methanol represents a significant entry point into the world of pyrimidine chemistry, blending structural intrigue with potential biological implications. Its study might contribute to uncovering new therapeutic pathways in modern medicine.

Synonyms
73-67-6
Toxopyrimidine
(4-Amino-2-methyl-5-pyrimidinyl)methanol
4-amino-5-hydroxymethyl-2-methylpyrimidine
(4-amino-2-methylpyrimidin-5-yl)methanol
pyramin
pyramine
Pyrazan
4-amino-2-methyl-5-pyrimidinemethanol
Atoxopyrimidine
5-Pyrimidinemethanol, 4-amino-2-methyl-
Oxymethylpyrimidine
Pyramine (VAN)
Pyramin (VAN)
OMPM
hydroxymethylpyrimidine
2-Methyl-4-amino-5-hydroxymethylpyrimidine
2-M-4-A-5-Hmp
CHEBI:16892
NSC 28247
UNII-G62V17J09J
PYRAMINE [VAN]
MFCD00849239
NSC-28247
TOXOPYRIMIDINE [MI]
Oprea1_032125
Pyramine (thiamine metabolite)
4-amino-2-methyl-5-hydroxymethylpyrimidine
DTXSID80223275
G62V17J09J
NSC28247
DB02022
TXP
(4-Amino-2-methyl-pyrimidin-5-yl)methanol
C01279
HMH
5-Pyrimidinemethanol,4-amino-2-methyl-
(4-?Amino-?2-?methyl-?5-?pyrimidinyl)?methanol(Toxopyrimidine)
EC-000.1414
HMP CPD
SCHEMBL479344
NChemBio.2007.13-comp6
CHEMBL1233354
4-A-2-MEP
DTXCID80145766
VUTBELPREDJDDH-UHFFFAOYSA-N
BBL100129
STK374214
ZINC00895559
AKOS002676258
CS-W006265
SB57336
4amino-5-hydroxymethyl-2-methylpyrimidine
BBV-00026439
DS-11140
FA142716
PD008215
2-methyl-4-amino-5-hydroxylmethylpyrimidine
6-amino-5-hydroxymethyl-2-methylpyrimidine
DB-005507
A2730
NS00068403
2-Methyl-4-amino-5-(hydroxymethyl)pyrimidine
5-Pyrimidinemethanol, 4-amino-2-methyl-(8CI)
EN300-135390
5-Pyrimidinemethanol, 4-amino-2-methyl-(8CI)(9CI)
Q27093111
5-Pyrimidinemethanol, 4-amino-2-methyl- (8CI)(9CI)
Z1198155379
806-933-7