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Flumetralin

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Identification
Molecular formula
C16H16F3N3O4P
CAS number
62924-70-3
IUPAC name
3-[fluoro(methyl)phosphoryl]oxy-2,2-dimethyl-butane
State
State

At room temperature, Flumetralin is typically found in a solid state, specifically as a crystalline powder.

Melting point (Celsius)
129.50
Melting point (Kelvin)
402.65
Boiling point (Celsius)
162.50
Boiling point (Kelvin)
435.65
General information
Molecular weight
335.20g/mol
Molar mass
335.1970g/mol
Density
1.1380g/cm3
Appearence

Flumetralin is a bright yellow powder and crystalline in nature. It is typically used as a plant growth regulator and is known for its bright coloration.

Comment on solubility

Solubility of 3-[fluoro(methyl)phosphoryl]oxy-2,2-dimethyl-butane

The solubility of 3-[fluoro(methyl)phosphoryl]oxy-2,2-dimethyl-butane is influenced by its unique structure and functional groups. Here are some key aspects to consider:

  • Polar vs. Nonpolar: This compound contains a phosphoryl group and a fluorine atom, which typically increases polarity. The presence of polar functional groups often enhances solubility in polar solvents, such as water.
  • Hydrogen Bonding: The phosphoryl group can participate in hydrogen bonding with water molecules, further promoting solubility.
  • Hydrophobic Character: The branched aliphatic structure may introduce some hydrophobic character, which could limit solubility in highly polar environments like water.
  • Solvent Interaction: It is likely to be more soluble in organic solvents, such as ethanol or acetone, due to the presence of its aliphatic components.

In conclusion, while the presence of polar groups suggests good solubility in polar solvents, the effect of the compound's hydrophobic regions may lead to variable solubility based on the specific solvent. Solubility studies would be essential to accurately determine the behavior of 3-[fluoro(methyl)phosphoryl]oxy-2,2-dimethyl-butane in various environments.

Interesting facts

Interesting Facts about 3-[fluoro(methyl)phosphoryl]oxy-2,2-dimethyl-butane

3-[fluoro(methyl)phosphoryl]oxy-2,2-dimethyl-butane is a fascinating compound that represents the intricate world of organophosphorus chemistry. This compound showcases the unique properties and reactivity that phosphorus-based compounds can exhibit. Here are some intriguing aspects:

  • Phosphoryl Group Significance: The phosphoryl group is essential in biochemistry, particularly in the formation of phosphoester bonds seen in DNA and RNA. This indicates potential applications in biological research.
  • Fluorine's Role: The presence of fluorine in the structure can impart unique electronic characteristics. Fluorinated compounds tend to have altered reactivity and stability, making them useful in specific industrial applications.
  • Potential Applications: Compounds like this may have applications in areas including pharmaceuticals, agrochemicals, and as intermediates in organic synthesis, highlighting their versatility in both commercial and research domains.
  • Structure-Activity Relationship: The incorporation of both a fluorinated and a phosphoryl group opens up pathways for studying how structural modifications influence biological activity, particularly in drug development.

Moreover, the synthesis of this compound may involve multi-step reactions, presenting a challenge that enables chemists to explore various reaction conditions and methods. As a compound with both practical significance and theoretical interest, 3-[fluoro(methyl)phosphoryl]oxy-2,2-dimethyl-butane truly embodies the complexity and beauty of modern chemical research.

In the words of celebrated chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." The study of compounds such as this one certainly contributes to a deeper understanding of chemistry and its applications.

Synonyms
SOMAN
Zoman
PMFP
Pinacolyl methylphosphonofluoridate
96-64-0
Pinacolyl methylfluorophosphonate
Pinacoloxymethylphosphoryl fluoride
Methyl pinacolyl phosphonofluoridate
Methyl pinacolyloxy phosphorylfluoride
CCRIS 3417
1,2,2-Trimethylpropyl methylphosphonofluoridate
Pinacolyl methylphosphonofluoride
Pynacolyl methylfluorophosphonate
HSDB 6764
3,3-Dimethyl-n-but-2-yl methylphosphonofluoridate
Phosphonofluoridic acid, methyl-, 1,2,2-trimethylpropyl ester
UNII-3OF3WXB67Q
3OF3WXB67Q
Pinacolyloxy methylphosphoryl fluoride
EA 1210
BRN 1928737
Phosphine oxide, fluoromethyl(1,2,2-trimethylpropoxy)-
Methylphosphonofluoridate, Pinacolyl
Methylphosphonofluoridic acid 1,2,2-trimethylpropyl ester
Methylfluorphosphorsaeurepinakolylester [German]
O-Pinacolyl methylphosphonofluoridate
Methylfluorphosphorsaeurepinakolylester
T.2107
SOMAN [MI]
1-Methyl-2,2-dimethylpropylmethylphosphonofluoridate
3-[fluoro(methyl)phosphoryl]oxy-2,2-dimethylbutane
Gd (chemical warfare agent)
2-Butanol, 3,3-dimethyl-, methylphosphonofluoridate
CHEMBL15910
CHEBI:9195
Methylphosphonofluoridic acid, 3,3-dimethyl-2-butyl ester
DTXSID2031906
1,2,2-Trimethylpropylester kyseliny methylfluorfosfonove [Czech]
1,2,2-Trimethylpropylester kyseliny methylfluorfosfonove
1,2,2-Trimethylpropoxyfluorophosphine oxide
3-[fluoro(methyl)phosphoryl]oxy-2,2-dimethyl-butane
PHOSPHONOFLUORIDIC ACID, P-METHYL-, 1,2,2-TRIMETHYLPROPYL ESTER
Methylfluorphosphorsaeurepinakolylester (German)
3-(fluoro(methyl)phosphoryl)oxy-2,2-dimethyl-butane
1,2,2-Trimethylpropylester kyseliny methylfluorfosfonove (Czech)
Agent GD
SOMAN.
Lethal Nerve Agent (GD)
3,3-dimethylbutan-2-yl methylphosphonofluoridate
SCHEMBL59654
(R)-Methylphosphonofluoridic acid 1,2,2-trimethylpropyl ester
G-SERIES NERVE AGENT GD
DTXCID0011906
BDBM50292572
AKOS006273455
3,3Dimethyl2butyl methylphosphonofluoridate
3,3Dimethylnbut2yl methylphosphonofluoridate
NS00076227
1,2,2Trimethylpropyl methylphosphonofluoridate
C07494
1Methyl2,2dimethylpropylmethylphosphonofluoridate
2Butanol, 3,3dimethyl, methylphosphonofluoridate
1,2,2-Trimethylpropyl methylphosphonofluoridoate #
Q408044
Methylphosphonofluoridic acid, 3,3dimethyl2butyl ester
Phosphine oxide, fluoromethyl(1,2,2trimethylpropoxy)
1,2,2Trimethylpropylester kyseliny methylfluorfosfonove
Methylphosphonofluoridic acid 1,2,2trimethylpropyl ester
Phosphonofluoridic acid, methyl, 1,2,2trimethylpropyl ester