Interesting facts
Interesting Facts about 1,3-Benzodioxole-5-Carbaldehyde
1,3-benzodioxole-5-carbaldehyde is a fascinating compound often studied in various fields of chemistry, including organic synthesis and medicinal chemistry. Below are some intriguing aspects of this compound:
- Structure and Functionality: This compound features both a benzenoid structure and a dioxole ring, providing unique structural properties that contribute to its reactivity and stability.
- Versatile Building Block: 1,3-benzodioxole-5-carbaldehyde serves as an important intermediate in the synthesis of more complex organic molecules, including pharmaceuticals and agrochemicals.
- Biological Activity: Some derivatives of this compound have shown promising biological activities, making it a candidate for further research in drug development.
- Natural Occurrence: Compounds related to benzodioxoles can be found in various plant species, underlining their significance in natural product chemistry and their potential health benefits.
- Research Interest: The study of 1,3-benzodioxole-5-carbaldehyde continues to attract attention, particularly in the search for new compounds with better efficacy against diseases.
In summary, 1,3-benzodioxole-5-carbaldehyde is more than just a simple chemical entity; it represents a connection between natural product chemistry and medicinal applications, demonstrating the versatility and importance of organic compounds in scientific exploration.
Synonyms
PIPERONAL
120-57-0
Heliotropine
Piperonyl aldehyde
Heliotropin
1,3-Benzodioxole-5-carbaldehyde
Piperonaldehyde
Piperonylaldehyde
3,4-Methylenedioxybenzaldehyde
Geliotropin
1,3-Benzodioxole-5-carboxaldehyde
3,4-(Methylenedioxy)benzaldehyde
5-Formyl-1,3-benzodioxole
Protocatechuic aldehyde methylene ether
3,4-Bis(methylenedioxy)benzaldehyde
3,4-Dihydroxybenzaldehyde methylene ketal
Dioxymethylene-protocatechuic aldehyde
3,4-Dimethylenedioxybenzaldehyde
Heliotropin (natural)
3,4-Methylene-dihydroxybenzaldehyde
FEMA No. 2911
Benzo[D][1,3]Dioxole-5-Carbaldehyde
Dioxymethylene protocatechuic aldehyde
NSC 26826
Benzaldehyde, 3,4-(methylenedioxy)-
CCRIS 5928
HSDB 581
EINECS 204-409-7
UNII-KE109YAK00
CHEBI:8240
KE109YAK00
DTXSID7025924
AI3-01198
NSC-26826
2H-1,3-Benzodioxole-5-Carbaldehyde
DTXCID505924
3,4-methylenedioxy-benzaldehyde
EC 204-409-7
3,4-METHYLEN-DIOXY-BENZALDEHYDE
1,3-BENZODIOXOLE-6-CARBOXALDEHYDE
DIOXYMETHYLENEPROTOCATECHUIC ALDEHYDE
benzo[1,3]dioxole-5-carbaldehyde
PIPERONAL (MART.)
PIPERONAL [MART.]
Piperonal DRUG PRECURSOR
2H-BENZO(3,4-D)-1,3-DIOXOLAN-5-YLFORMALDEHYDE
5-Formylbenzodioxole
heliotrin
Piperonale
Piperanal
Blue P
Piperonal, 8CI
Piperonal, 99%
PIPERONAL [FCC]
Heliotropine (piperonal)
PIPERONAL [MI]
PIPERONAL [FHFI]
PIPERONAL [HSDB]
4-methylenedioxybenzaldehyde
PIPERONAL [WHO-DD]
SCHEMBL29318
Piperonal, analytical standard
3,4-Methylendioxy-benzaldehyde
Piperonal crystals (Synthetic)
CHEMBL271663
3,4 -methylenedioxybenzaldehyde
3,4-methylene-dioxybenzaldehyde
3,4-methylenedioxy benzaldehyde
1,3-benzodioxol-5-carbaldehyde
Piperonal, natural, 98%, FG
FEMA 2911
Benzaldehyde,4-(methylenedioxy)-
benzo[1,3]dioxol-5-carbaldehyde
3,4-methylenedihydroxybenzaldehyde
3,4-(methylenedioxy)-benzaldehyde
BDBM153298
benzo-1,3-dioxole-5-carbaldehyde
Piperonal, >=99%, FCC, FG
WLN: T56 BO DO CHJ GVH
3, 4-(Methylenedioxy)benzaldehyde
NSC26826
1,3-Benzodioxole-5-carbaldehyde #
benzo[1,3]dioxole-5-carboxaldehyde
Tox21_200120
5-FORMYL-1,3-BENZODIOXOLANE
BBL007668
MFCD00005828
STK188426
3, 4-Bis(methylenedioxy)benzaldehyde
AKOS002662846
FP44782
NCGC00091137-01
NCGC00091137-02
NCGC00257674-01
1,3-Benzodioxole-5-carboxaldehyde, 9CI
AC-11587
benzo[d]-1,3-dioxolane-5-carboxaldehyde
CAS-120-57-0
3,4-Methylenedioxybenzaldehyde (Piperonal)
DB-021956
Heliotropin;3,4-(Methylenedioxy)benzaldehyde
NS00001813
P0456
PIPERONAL (CONSTITUENT OF BLACK PEPPER)
Q418985
PIPERONAL (CONSTITUENT OF BLACK PEPPER) [DSC]
InChI=1/C8H6O3/c9-4-6-1-2-7-8(3-6)11-5-10-7/h1-4H,5H
204-409-7
5XC
Solubility of 1,3-benzodioxole-5-carbaldehyde
1,3-benzodioxole-5-carbaldehyde, often referred to as a versatile aromatic compound, exhibits notable solubility characteristics that are essential for its applications in various chemical processes. Understanding its solubility can be pivotal for researchers and industrial chemists alike.
Solubility Profile
In summary, while 1,3-benzodioxole-5-carbaldehyde is soluble in a range of organic solvents, its hydrophobic characteristics make it less soluble in polar solvents like water. This solubility behavior can significantly influence its reactivity and applications in synthesis, making it a crucial consideration for chemists working with this intriguing compound.