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Allyl 2-(2-allyloxycarbonyloxyethoxy)ethyl carbonate

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Identification
Molecular formula
C13H18O7
CAS number
164996-13-4
IUPAC name
allyl 2-(2-allyloxycarbonyloxyethoxy)ethyl carbonate
State
State

At room temperature, Allyl 2-(2-allyloxycarbonyloxyethoxy)ethyl carbonate is a liquid.

Melting point (Celsius)
-30.00
Melting point (Kelvin)
243.20
Boiling point (Celsius)
398.90
Boiling point (Kelvin)
672.10
General information
Molecular weight
258.27g/mol
Molar mass
258.2740g/mol
Density
1.1188g/cm3
Appearence

This compound typically appears as a clear, colorless to pale yellow liquid. It is known to be viscous and may possess a characteristic ester odor.

Comment on solubility

Solubility of Allyl 2-(2-allyloxycarbonyloxyethoxy)ethyl Carbonate

The solubility of allyl 2-(2-allyloxycarbonyloxyethoxy)ethyl carbonate in various solvents can be intriguing due to its unique chemical structure. This compound is characterized by the presence of two ether linkages and carbonate functional groups, which influence its solubility behavior.

Key Points Regarding Solubility:

  • Polar vs. Non-polar Solvents: Due to the ether groups, this compound is expected to have moderate solubility in polar solvents such as ethanol and methanol, while maintaining reasonable compatibility with non-polar solvents like hexane.
  • Temperature Effects: Generally, as the temperature increases, the solubility of organic compounds can also increase, making heating a potential method for improving solubility in experimental scenarios.
  • Presence of Functional Groups: The carbonate group enhances hydrogen-bonding capabilities, contributing positively to solubility in polar environments.

Overall, while specific solubility data for allyl 2-(2-allyloxycarbonyloxyethoxy)ethyl carbonate in individual solvents may vary, it is likely to exhibit a broad range of solubility profiles, accentuated by its unique structural features. It is also advisable to perform empirical tests to determine the precise solubility characteristics for practical applications.

Interesting facts

Interesting Facts about Allyl 2-(2-allyloxycarbonyloxyethoxy)ethyl Carbonate

Allyl 2-(2-allyloxycarbonyloxyethoxy)ethyl carbonate is a fascinating compound in the realm of organic chemistry, particularly due to its unique structure and potential applications. Here are some captivating aspects to explore:

  • Versatile Structure: The compound features an allyl group, which is well-known for its reactivity in various organic transformations. Its structure promotes interesting interactions with other compounds, making it valuable in both research and industrial applications.
  • Polymer Development: This carbonated ester is often utilized as a monomer in the synthesis of polymers. Its ability to undergo polymerization reactions allows scientists to create materials with tailored properties, which are essential in many fields, from coatings to biomedical applications.
  • Functionalization Potential: The presence of allyloxy and carbonyl groups in the structure facilitates *functionalization*. This allows chemists to modify the compound for specific purposes, enhancing its reactivity and stability in various environments.
  • Applications in Drug Delivery: Due to its chemical characteristics, this compound shows promise in the realm of drug delivery systems. The ability to modify its structure can lead to enhanced drug solubility and controlled release, which are crucial in developing effective therapies.
  • Reactivity Insights: The reactivity of allyl compounds is a significant area of study. According to noted chemists, "the unique reactivity of the allyl group often leads to unexpected results in synthetic reactions," highlighting the compound's role in advancing organic synthesis methodologies.

As chemistry continues to evolve, compounds like allyl 2-(2-allyloxycarbonyloxyethoxy)ethyl carbonate will undoubtedly play vital roles in innovation, particularly in developing functional materials and advanced therapeutic strategies.

Synonyms
142-22-3
Diallyl 2,2'-oxydiethyl dicarbonate
DIALLYL DIGLYCOL CARBONATE
Allyl diglycol carbonate
Diallyl glycol carbonate
CR 39
Nouryset 200
Transallyl CR 39
Diethylene glycol bis(allylcarbonate)
High ADC-CR 39
RAV 7N
Carbonic acid, oxydiethylene diallyl ester
Diethylene glycol diallyl dicarbonate
Diallyl oxydiethylene dicarbonate
HSDB 5638
TS 16
UNII-AJ5T8CR88I
NSC 5246
EINECS 205-528-7
2,5,8,10-Tetraoxatridec-12-enoic acid, 9-oxo-, 2-propenyl ester
BRN 1803874
Diethylene glycol, bis(allyl carbonate)
2-(2-prop-2-enoxycarbonyloxyethoxy)ethyl prop-2-enyl carbonate
Oxydiethylenedicarbonic acid diallyl ester
Ethanol, 2,2'-oxybis-, bis(2-propenyl carbonate)
AI3-07498
Carbonic acid, allyl ester, diester with diethylene glycol
Carbonic acid, oxydi-2,1-ethanediyl di-2-propenyl ester
NSC-5246
Diallyl 2,2/'-oxydiethyl dicarbonate
diallyl (oxybis(ethane-2,1-diyl)) bis(carbonate)
AJ5T8CR88I
DTXSID7027095
EC 205-528-7
4-03-00-00012 (Beilstein Handbook Reference)
Diethylene glycol bis(allyl carbonate)
01M
DIALLYL DIGLYCOL CARBONATE [HSDB]
diallyl oxydiethane-2,1-diyl biscarbonate
2,5,8-trioxa-nonanedioic acid diallyl ester
2,5,8,10-Tetraoxatridec-12-enoic acid, 9-oxo-, 2-propen-1-yl ester
Baryotrak
Tastrak
Allur
Patras
Seiko Plax
Lantrak 1
Lantrak 2
Harzlas TD 1
Homalite 911
ORMA
PADC
PADC compound
ORMA 1000
CR 307
PM 355
PM 500
PM 600
diallylglycol carbonate
High ADCCR 39
allyl-diglycol-carbonate
SCHEMBL50692
CR39
DTXCID407095
NSC5246
WLN: 1U2OVO2O2OVO2U1
JHQVCQDWGSXTFE-UHFFFAOYSA-N
CR-39
UN3237
AKOS025311124
Diallyl 2,2\'-oxydiethyl dicarbonate
DB-042614
NS00008879
Carbonic acid,1-ethanediyl di-2-propenyl ester
Ethanol, 2,2'oxybis, bis(2propenyl carbonate)
Ethanol,2'-oxybis-, bis(2-propenyl carbonate)
Carbonic acid, oxydiethylene diallyl ester (8CI)
Q409703
Carbonic acid, oxydi2,1ethanediyl di2propenyl ester
CARBONIC ACID, OXYDIETHYLENEDI-, DIALLYL ESTER
carbonic acid allyl 2-(2-allyloxycarbonyloxyethoxy)ethyl ester
2,8,10-Tetraoxatridec-12-enoic acid, 9-oxo-, 2-propenyl ester
2,5,8,10-TETRAOXATRIDEC-12-ENOIC ACID, 9-OXO-, 2-PROPEN-1- YL ESTER