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Triphosgene

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Identification
Molecular formula
C3Cl6O3
CAS number
32315-10-9
IUPAC name
2-(2-chlorocarbonyloxyethoxy)ethyl carbonochloridate
State
State

At room temperature, triphosgene is in a solid state.

Melting point (Celsius)
79.30
Melting point (Kelvin)
352.45
Boiling point (Celsius)
206.00
Boiling point (Kelvin)
479.15
General information
Molecular weight
296.56g/mol
Molar mass
296.5560g/mol
Density
1.5450g/cm3
Appearence

Triphosgene is a crystalline white solid at room temperature. It has a distinctive appearance that may resemble powdered sugar or other fine crystalline powders. Handle with caution as it has hazardous properties.

Comment on solubility

Solubility of 2-(2-chlorocarbonyloxyethoxy)ethyl carbonochloridate

The solubility of 2-(2-chlorocarbonyloxyethoxy)ethyl carbonochloridate can be influenced by a variety of factors. Understanding these factors can provide insights into its behavior in different environments. Here are some important points to consider:

  • Polarity: The presence of carbonyl and ether functional groups suggests that the compound may exhibit moderate polarity, which can affect its interaction with solvents.
  • Solvent Compatibility: It is likely to be more soluble in polar aprotic solvents or organic solvents, such as acetone or ethyl acetate, rather than in water due to its structural characteristics.
  • Temperature Influence: As with many compounds, increasing the temperature may enhance solubility by providing more energy to overcome solute-solvent interactions.
  • pH Dependence: The solubility might also vary with changing pH levels, particularly if the compound can undergo protonation or deprotonation.

In conclusion, while specific solubility data for 2-(2-chlorocarbonyloxyethoxy)ethyl carbonochloridate may not be universally available, awareness of its structural attributes and the factors influencing solubility can guide users in selecting compatible solvents for practical applications.

Interesting facts

Interesting Facts about 2-(2-Chlorocarbonyloxyethoxy)ethyl Carbonochloridate

2-(2-Chlorocarbonyloxyethoxy)ethyl carbonochloridate is a fascinating compound in the realm of organic chemistry, particularly known for its potential applications in various chemical syntheses. Here are some intriguing insights:

  • Functional Versatility: This compound contains multiple functional groups, specifically an ester and an acid chloride, which can participate in a variety of chemical reactions, making it exceptionally versatile in synthetic pathways.
  • Intermediary Role: It serves as a crucial intermediate in the synthesis of other complex molecules. This makes it invaluable in pharmaceutical chemistry, where producing intricate compounds efficiently is essential.
  • Reactivity: The presence of a carbonochloridate group suggests that this compound is quite reactive, particularly towards nucleophiles. This can lead to the formation of new bonds and compounds, highlighting its utility in organic synthesis.
  • Applications: While research is still ongoing, its potential applications extend into agrochemicals and DNA synthesis, where its reactivity could facilitate the development of new agricultural agents or genetic materials.
  • Environmental Considerations: As with many chlorinated compounds, understanding the environmental impact and degradation pathways of 2-(2-chlorocarbonyloxyethoxy)ethyl carbonochloridate is crucial, particularly in light of increasing regulations surrounding chlorinated chemicals.

As a compound that exemplifies the complexity and versatility of organic molecules, 2-(2-chlorocarbonyloxyethoxy)ethyl carbonochloridate continues to be a subject of interest for both research and practical applications in chemistry. Its unique structure offers a glimpse into the intricate world of organic synthesis where small changes can lead to significant outcomes.

Synonyms
Oxydiethylene bis(chloroformate)
106-75-2
Diglycol chlorformate
Diglycol chloroformate
Oxydiethylene chloroformate
Diethylene glycol chloroformate
Oxydiethylenebis(chloroformate)
DIETHYLENE GLYCOL, BISCHLOROFORMATE
2-(2-carbonochloridoyloxyethoxy)ethyl carbonochloridate
HSDB 5374
Carbonochloridic acid, oxydi-2,1-ethanediyl ester
Formic acid, chloro-, oxydiethylene ester
1,5-Bis((chlorocarbonyl)oxy)-3-oxapentane
NSC 2346
Diethylene glycol bis(chloroformate)
EINECS 203-430-9
BRN 1812829
AI3-26267
0O453X86MX
NSC-2346
Formic acid, chloro-, diester with diethylene glycol
Carbonochloridic acid, C,C'-(oxydi-2,1-ethanediyl) ester
DTXSID2026739
Diethyleneglycolbis(chloroformatE)
Diethylene glycol, bis(Chloroformate)
Carbonochloridic acid,C,C'-(oxydi-2,1-ethanediyl) ester
BIS(2-CHLOROCARBONYLOXYETHYL)ETHER
DIETHLYLENE GLYCOL BIS CHLOROFORMATE
1,5-BIS((CHLOROCARBONYL)OXY)-3-OXAPENTANE [HSDB]
Diethylene glycol bis-chloroformate
1,5-Bis[(chlorocarbonyl)oxy]-3-oxapentane
oxydiethane-2,1-diyl dichlorocarbonate
UNII-0O453X86MX
MFCD00018800
Oxydiethylenbis(chlorformiat)
DTXCID506739
SCHEMBL1063406
CHEMBL3188675
Formic acid, oxydiethylene ester
NSC2346
XFSAZBKSWGOXRH-UHFFFAOYSA-N
Formic acid, chloro-, diester with diethylene glycol (6CI)
Tox21_301037
AKOS025310981
1,5Bis((chlorocarbonyl)oxy)3oxapentane
Carbonochloridic acid,1-ethanediyl ester
Formic acid, chloro, oxydiethylene ester
NCGC00248265-01
NCGC00254939-01
CAS-106-75-2
NS00019762
Carbonochloridic acid, oxydi2,1ethanediyl ester
Carbonochloridic acid oxydi-2,1-ethanediyl ester
Formic acid, chloro, diester with diethylene glycol
Q27237021
Formic acid, chloro, diester with diethylene glycol (6CI)
203-430-9