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Fluoromethylphosphate

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Identification
Molecular formula
C4H10FO4P
CAS number
14831-13-5
IUPAC name
2-[fluoro(methyl)phosphoryl]oxypropane
State
State

At room temperature, fluoromethylphosphate exists as a liquid.

Melting point (Celsius)
-28.00
Melting point (Kelvin)
245.15
Boiling point (Celsius)
125.00
Boiling point (Kelvin)
398.15
General information
Molecular weight
125.07g/mol
Molar mass
125.0730g/mol
Density
1.2000g/cm3
Appearence

Fluoromethylphosphate is typically a colorless liquid.

Comment on solubility

Solubility of 2-[fluoro(methyl)phosphoryl]oxypropane

The solubility of 2-[fluoro(methyl)phosphoryl]oxypropane can be described as follows:

  • Polarity: The presence of both the phosphoryl group and the fluorine atom contributes to the molecule's overall polarity. This polarity can enhance its interaction with polar solvents, such as water.
  • Solvent Interaction: Due to its polar nature, 2-[fluoro(methyl)phosphoryl]oxypropane is expected to be soluble in polar organic solvents.
  • Hydrogen Bonding: The molecule has the potential to engage in hydrogen bonding with polar solvents, which may further promote solubility.

However, the specific solubility in various solvents has not been extensively documented, making it essential to conduct empirical testing to determine precise solubility characteristics.

In summary, while we can infer that 2-[fluoro(methyl)phosphoryl]oxypropane exhibits some degree of solubility in polar environments, empirical data is crucial for an accurate understanding.

Interesting facts

Interesting Facts About 2-[Fluoro(methyl)phosphoryl]oxypropane

2-[Fluoro(methyl)phosphoryl]oxypropane is a fascinating compound in the field of organic and inorganic chemistry, representing a significant advancement in the study of organophosphorus compounds. This compound belongs to a category known for its diverse applications and essential roles in various fields.

Key Characteristics:

  • Functionality: The presence of the fluorine atom in the compound enhances its reactivity and biological activity, which can be crucial for developing pesticides and pharmaceuticals.
  • Phosphorylation: The phosphoryl group contributes to the compound's ability to form important bonds with biological molecules, impacting enzyme activity and metabolic pathways.
  • Stability: Organophosphorus compounds like this one are known for their stability under certain conditions, making them valuable in practical applications.

Applications and Relevance:

This compound has notable applications in:

  • **Agricultural Chemistry**: Widely explored as a pesticide due to its efficacy against pests while remaining effective in small doses.
  • **Drug Development**: Research indicates its potential as a lead compound in synthesizing drugs that target specific biological pathways.
  • **Chemical Synthesis**: Acts as an important intermediate in industrial organic synthesis, expanding its utility across various chemical processes.

As a scientist or a chemistry student, understanding compounds like 2-[fluoro(methyl)phosphoryl]oxypropane highlights the intricate balance between chemistry and biology, emphasizing the importance of phosphorus and its compounds in both nature and synthetic applications.
Remember as Albert Einstein said, "The whole of science is nothing more than a refinement of everyday thinking." This compound serves as a perfect example of how complex structures emerge from fundamental chemical principles.

Synonyms
SARIN
Sarin II
Trilone 46
107-44-8
IMPF
O-Isopropyl methylphosphonofluoridate
Isopropyl methylfluorophosphate
Isopropyl methylphosphonofluoridate
Sarin.
2-[fluoro(methyl)phosphoryl]oxypropane
Isopropyl methanefluorophosphonate
Isopropoxymethylphosphoryl fluoride
Isopropyl-methyl-phosphoryl fluoride
Methylphosphonofluoridic acid isopropyl ester
CCRIS 3416
EA 1208
TL 1618
Isopropoxymethylphoshoryl fluoride
Phosphine oxide, fluoroisopropoxymethyl-
HSDB 6382
UNII-B4XG72QGFM
Phosphonofluoridic acid, methyl-, isopropyl ester
B4XG72QGFM
Phosphonofluoridic acid, methyl-, 1-methylethyl ester
T-144
Phosphoric acid, methylfluoro-, isopropyl ester
T-2106
Methylphosphonofluoridic acid 1-methylethyl ester
BRN 1750114
(+-)-Isopropyl methylphosphonofluoridate
Isopropyl methylfluorophosphonate
CHEBI:75701
Methlyfluorophosphonic acid isopropyl ester
Isopropylester kyseliny methylfluorfosfonove
Methylphosphonofluoride acid, isopropyl ester
1-Methylethyl (+-)-methylphosphonofluoridate
Methylfluorphosphorsaeureisopropylester
GB
MFI
Phosphonofluoridic acid, methyl-, isopropyl ester, (+-)-
DTXSID0042371
O-Isopropyl methylfluorophosphonate
4-04-00-03507 (Beilstein Handbook Reference)
1-Methylethyl methylphosphonofluoridate
Phosphonofluoridic acid, P-methyl-, 1-methylethyl ester
Methylfluorophosphoric acid isopropyl ester
SARIN (MART.)
SARIN [MART.]
(+/-)-ISOPROPYL METHYLPHOSPHONOFLUORIDATE
PHOSPHONOFLUORIDIC ACID, METHYL-, ISOPROPYL ESTER, (+/-)-
Gas, Sarin
o-Isopropylmethyl Phosphonofluoridate
ortho-Isopropylmethyl Phosphonofluoridate
racemic sarin
Zarin
Methylfluorphosphorsaeureisopropylester [German]
S-Sarin
Agent GB
Isopropylester kyseliny methylfluorfosfonove [Czech]
o Isopropylmethyl Phosphonofluoridate
(RS)-sarin
Phosphonofluoridate, o-Isopropylmethyl
ortho Isopropylmethyl Phosphonofluoridate
(+-)-sarin
Phosphonofluoridate, ortho-Isopropylmethyl
SARIN [HSDB]
SARIN [MI]
Methylfluoro-isopropyl ester
(.+/-.)-Sarin
SCHEMBL50256
Fluoroisopropoxymethylphosphine
CHEMBL509554
DTXCID8022371
CHEBI:75873
DTXSID70897222
GB (CHEMICAL WARFARE AGENT)
BDBM50027343
propan-2-yl methylphosphonofluoridate
Isopropyl methylphosphonofluoridoate #
rac-isopropyl methylphosphonofluoridate
AKOS006273454
Methylfluorphosphorsaeureisopropyl ester
(RS)-isopropyl methylphosphonofluoridate
rac-propan-2-yl methylphosphonofluoridate
T144
NS00075366
NS00075518
PHOSPHINE OXIDE, FLUOROISOPROPOXYMETHYL
Fluoroisopropoxymethyl phospline phosphine oxide
Methylphosphonofluoridic acid 1-methyl-ethyl ester
Q187695