Interesting facts
Interesting Facts about Diallyl Benzene-1,2-dicarboxylate
Diallyl benzene-1,2-dicarboxylate is a compound that holds significance in both organic chemistry and industrial applications. Here are some captivating insights about this compound:
- Chemical Structure: The compound features a diallyl group, which consists of two allyl groups attached to a central benzene ring that is further substituted with two carboxylate groups. This unique structure contributes to its reactivity and functionality.
- Versatile Uses: Diallyl benzene-1,2-dicarboxylate is often utilized in the production of specialty chemicals and polymers. Its ability to undergo polymerization makes it a valuable building block for creating various materials.
- Green Chemistry: The compound is increasingly studied in the context of green chemistry. Its synthesis can be optimized to minimize waste and energy consumption, aligning with sustainable practices in chemical production.
- Reactivity: Diallyl benzene-1,2-dicarboxylate can participate in various chemical reactions, including Diels-Alder reactions, making it a fascinating subject for researchers aiming to explore new synthetic pathways.
- Biological Activities: Preliminary studies suggest potential biological activities associated with this compound. Its derivatives may exhibit antioxidant and antimicrobial properties, opening avenues for pharmaceutical research.
In summary, diallyl benzene-1,2-dicarboxylate exemplifies how organic compounds can serve as crucial intermediates in both industrial applications and research innovations.
Synonyms
DIALLYL PHTHALATE
131-17-9
Allyl phthalate
Diallylphthalate
Dapon 35
Dapon R
Phthalic acid, diallyl ester
1,2-Benzenedicarboxylic acid, di-2-propenyl ester
Phthalic Acid Diallyl Ester
o-Phthalic acid, diallyl ester
1,2-Benzenedicarboxylic acid, 1,2-di-2-propen-1-yl ester
NCI-C50657
Diallylester kyseliny ftalove
NSC 7667
CCRIS 1361
Di-2-propenyl 1,2-benzenedicarboxylate
HSDB 4169
Diallylester phthalic acid
DAP monomer
UNII-F79L0UL6ST
bis(prop-2-enyl) benzene-1,2-dicarboxylate
EINECS 205-016-3
F79L0UL6ST
Diallylester kyseliny ftalove [Czech]
BRN 1880877
phthalic acid, bis-allyl ester
DTXSID7020392
AI3-02574
NSC-7667
143318-73-4
Diallyl ester o-phthalic acid
DTXCID70392
Diallyl ester of phthalic acid
RX 1-501N (Salt/Mix)
DIALLYL PHTHALATE [HSDB]
EC 205-016-3
DIPROP-2-ENYL BENZENE-1,2-DICARBOXYLATE
RX 3-1-530 (Salt/Mix)
4-09-00-03188 (Beilstein Handbook Reference)
Nonflammable decobest DA (Salt/Mix)
1,2-bis(prop-2-en-1-yl) benzene-1,2-dicarboxylate
Diallylester Kyseliny Ftalove (Czech)
205-016-3
CAS-131-17-9
MFCD00008646
o-phthalic acid diallyl ester
di-allyl phthalate
DAPPU
Diallyl phthalic acid
DAP-M
Nonflammable decobest DA
Diallyl phthalate, 97%
SCHEMBL15174
MLS002415725
oPhthalic acid, diallyl ester
WLN: 1U2OVR BVO2U1
CHEMBL1329372
NSC7667
HMS2267F17
Di2propenyl 1,2benzenedicarboxylate
Tox21_201961
Tox21_300135
DT 170
Phthalic acid, diallyl ester (8CI)
Diallyl phthalate, analytical standard
AKOS015891274
NCGC00091365-01
NCGC00091365-02
NCGC00091365-03
NCGC00091365-04
NCGC00254197-01
NCGC00259510-01
BS-14891
SMR001253767
NS00011513
P0290
1,2Benzenedicarboxylic acid, di2propenyl ester
F87052
Q2161731
1,2-Benzenedicarboxylic acid 1,2-di-2-propen-1-yl ester
Diallyl ortho-phthalate;1,2Benzenedicarboxylic acid di-2-propenyl ester;Phthalic acid,bis-allyl ester;Phthalic acid diallyl ester;
Solubility of Diallyl Benzene-1,2-dicarboxylate
Diallyl benzene-1,2-dicarboxylate, known for its unique structure, exhibits intriguing solubility characteristics that can be influenced by several factors. Understanding its solubility is crucial for applications in organic synthesis and materials science.
Solubility Properties:
In summary, the solubility of diallyl benzene-1,2-dicarboxylate is influenced by its chemical structure and the nature of the solvent used. It is vital to consider these factors for effective use in various chemical processes. As the saying goes, "like dissolves like," which rings especially true for this compound's solubility behavior.