Adrenaline Tartarate
- Molecular formula
- C13H19NO9
- CAS Number
- 51-42-3
- IUPAC Name
- 4-(2-amino-1-hydroxy-ethyl)benzene-1,2-diol;(2R,3R)-2,3-dihydroxybutanedioic acid
- Molecular Weight
- 333.29g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.6000g/cm3
- Synonyms
- 1, 2-Benzenediol, 4-(2-amino-1-hydroxyethyl)-, (2R, 3R)-2, 3-dihydroxybutanedioate (1:1) (salt)
Identification
Exploring 4-(2-amino-1-hydroxy-ethyl)benzene-1,2-diol and (2R,3R)-2,3-dihydroxybutanedioic acid
The compound known as 4-(2-amino-1-hydroxy-ethyl)benzene-1,2-diol, in conjunction with (2R,3R)-2,3-dihydroxybutanedioic acid, presents a fascinating amalgamation of functionalities that contribute to various biological and chemical processes. Here are some intriguing aspects of this compound:
- Biological Importance: The amino group and hydroxy groups present in this compound play a crucial role in the development of pharmaceuticals and bioactive molecules. These functionalities are involved in various biochemical pathways, including those related to enzymatic activities and metabolic processes.
- Redox Properties: The presence of phenolic hydroxyl groups in 4-(2-amino-1-hydroxy-ethyl)benzene-1,2-diol allows for potential redox reactions, making it interesting for applications in creating antioxidants or in electrochemical studies.
- Sugar Acid Relation: (2R,3R)-2,3-dihydroxybutanedioic acid, related to natural sugars, exhibits properties that are relevant in biochemistry, particularly in the synthesis of sugar derivatives essential for cellular functions.
- Complex Formation: This compound can interact with metal ions, forming complexes that may be harnessed in fields such as catalysis and materials science, showcasing its versatility in chemical applications.
Furthermore, it is noteworthy that the stereochemistry of (2R,3R)-2,3-dihydroxybutanedioic acid enhances its biological significance. According to many studies, compounds with specific stereoisomer configurations often exhibit distinctive biological activities. Thus, understanding the precise configuration can lead to advancements in targeted therapeutics.
In summary, the combination of functional groups and structural features in 4-(2-amino-1-hydroxy-ethyl)benzene-1,2-diol and (2R,3R)-2,3-dihydroxybutanedioic acid not only contributes to its unique chemical properties but also opens avenues for further research and applications in chemistry and biomedicine.