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(2,3-dihydroxy-4-methylsulfonyloxy-butyl) methanesulfonate

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Identification
Molecular formula
C7H14O9S2
CAS number
50874-52-3
IUPAC name
(2,3-dihydroxy-4-methylsulfonyloxy-butyl) methanesulfonate
State
State

At room temperature, (2,3-dihydroxy-4-methylsulfonyloxy-butyl) methanesulfonate is typically found in a liquid state.

Melting point (Celsius)
18.40
Melting point (Kelvin)
291.55
Boiling point (Celsius)
352.15
Boiling point (Kelvin)
625.30
General information
Molecular weight
242.27g/mol
Molar mass
242.2740g/mol
Density
1.3210g/cm3
Appearence

The compound is known to appear as a colorless or pale yellow liquid. It may have a faint sulfurous odor due to the sulfonate groups present in the structure.

Comment on solubility

Solubility of (2,3-dihydroxy-4-methylsulfonyloxy-butyl) methanesulfonate

The solubility of (2,3-dihydroxy-4-methylsulfonyloxy-butyl) methanesulfonate is influenced by its molecular structure and functional groups. Here are some key aspects to consider:

  • Polar Characteristics: The presence of hydroxyl groups (-OH) within the compound suggests a tendency to interact favorably with polar solvents such as water.
  • Sulfonyloxy Functional Group: The sulfonate group is likely to enhance solubility due to its ionic nature, which promotes dissolution in aqueous environments.
  • Hydrogen Bonding: The ability of the compound to form hydrogen bonds can significantly affect its solubility, allowing it to disperse in compatible solvents.

Overall, it can be anticipated that (2,3-dihydroxy-4-methylsulfonyloxy-butyl) methanesulfonate displays notable solubility characteristics, particularly in polar solvents. This makes it a versatile compound within various applications where solubility is a critical factor.

Interesting facts

Interesting Facts about (2,3-Dihydroxy-4-methylsulfonyloxy-butyl) Methanesulfonate

(2,3-Dihydroxy-4-methylsulfonyloxy-butyl) methanesulfonate is a fascinating compound that showcases the intersection of chemistry and biochemistry. Here are some engaging insights:

  • Functional Groups: This compound includes several significant functional groups, such as alcohols (hydroxy groups) and sulfonates. These groups play crucial roles in chemical reactivity and interactions within biological systems.
  • Potential Applications: Given its unique structure, this compound may have potential applications in medicinal chemistry, especially in drug synthesis. The presence of hydroxyl and sulfonyl groups can enhance solubility and bioavailability.
  • Biochemical Importance: Hydroxy groups are essential for hydrogen bonding, which is fundamental in biochemical interactions, including enzyme-substrate binding and protein folding.
  • Research Interests: Compounds of this nature are often subjects of research focused on their roles in cellular processes, particularly concerning how they might participate in signaling pathways or metabolic reactions.
  • Notable Reactions: The methanesulfonate portion indicates that this compound might be involved in nucleophilic substitution reactions, which are key mechanisms in organic synthesis.
  • Environmental Considerations: Understanding the stability and reactivity of compounds like this one can contribute to fields such as environmental chemistry, where the fate of organic pollutants is analyzed.

The interplay of its structural components makes (2,3-dihydroxy-4-methylsulfonyloxy-butyl) methanesulfonate an exciting compound in the study of both synthetic and natural processes. As stated, “The beauty of chemistry lies in its complexity, and compounds like this illustrate just how intricately molecules are designed for specific functions.”

Synonyms
Tresulfan
Erythritol, 1,4-dimethanesulfonate
Dihydroxymyleran
Dihydroxybusulfan
L-Threityl dimesylate
Dimesyl-meso-erythritol
1,4-Bis(methylsulfonyloxy)threitol
Threitol 1,4-bis(methanesulfonate)
NCGC00181153-01
1,4-Di(methanesulfonate)erythritol
CB 2562
CB 40069
1,4-Bis mesyl ester of D-threitol
1,2,3,4-Butanetetrol, 1,4-dimethanesulfonate, (R*,S*)-
CB 40065
Erythritol, dimesyl-, meso-
NSC 39069;Treosulphan
NSC 94160
DTXCID106173
Erythritol, 1,4-bis(methanesulfonate)
(2,3-dihydroxy-4-methylsulfonyloxybutyl) methanesulfonate
Threitol, 1,4-dimethanesulfonate
Threitol-1,4-bismethanesulfonate, meso-
Treosulfa
NSC39069
1,4-Bis(methanesulfonyloxy)-2,3-butanediol
21106-06-9
ERYTHRITOL, 1,4-DIMETHANESULFONATE, (meso)-
1,2,3,4-Butanetetrol, 1,4-dimethanesulfonate, (R-(R*,S*))-
(2S,4-bismethanesulfonate
SCHEMBL8142
NCIOpen2_006538
Threitol,4-dimethanesulfonate
GTPL8281
CHEMBL2358556
1,4-DimethanesulfonateL-Threitol
Threitol,4-dimethanesulfonate, L-
BCP31509
D-Threitol,4-bis(methanesulfonate)
L-Threitol,4-bis(methanesulfonate)
NSC39068
Tox21_112757
NSC-39068
NSC260698
NSC 260698
NSC-260698
L-Threitol-1, 4-bis(methanesulfonate)
Threitol,4-dimethanesulfonate, L-(+)-
1,4-DimethanesulfonateL-(+ )-Threitol
L-Threitol, 1, 4-bis(methanesulfonate)
1,4-Dimethanesulfonate(2S,3S)-Threitol
CAS-299-75-2
Threitol,4-dimethanesulfonate, (2S,3S)-
NS00007093
E83713
2,3-dihydroxybutane-1,4-diyl dimethanesulfonate
Q7838652
1,2,3,4-Butanetetrol, 1,4-dimethanesulfonate, (R*,R*)-
1,3,4-Butanetetrol, 1,4-dimethanesulfonate, (R*,R*)-
2,3-dihydroxy-4-(methanesulfonyloxy)butyl methanesulfonate
NSC 39069; NSC39069; NSC-39069;Treosulphan;Ovastat
1,3,4-Butanetetrol, 1,4-dimethanesulfonate, [R-(R*,R*)]-
1,3,4-Butanetetrol, 1,4-dimethanesulfonate, [S-(R*,R*)]-