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Acetaldehyde

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Identification
Molecular formula
C2H4O
CAS number
75-07-0
IUPAC name
acetoxymethyl 2-[N-[2-(acetoxymethoxy)-2-oxo-ethyl]-2-[2-[2-[bis[2-(acetoxymethoxy)-2-oxo-ethyl]amino]phenoxy]ethoxy]anilino]acetate
State
State

Acetaldehyde exists as a volatile liquid at room temperature but can also be present in a gaseous state if not contained. It is known for its characteristic pungent odor.

Melting point (Celsius)
-123.50
Melting point (Kelvin)
149.65
Boiling point (Celsius)
20.20
Boiling point (Kelvin)
293.35
General information
Molecular weight
44.05g/mol
Molar mass
44.0530g/mol
Density
0.7840g/cm3
Appearence

Acetaldehyde is a colorless, volatile liquid with a pungent, fruity odor. It can appear as a gaseous form at room temperature or a volatile liquid when slightly cooled. The substance is flammable and miscible with water.

Comment on solubility

Solubility of Acetoxymethyl 2-[N-[2-(acetoxymethoxy)-2-oxo-ethyl]-2-[2-[2-[bis[2-(acetoxymethoxy)-2-oxo-ethyl]amino]phenoxy]ethoxy]anilino]acetate

The compound acetoxymethyl 2-[N-[2-(acetoxymethoxy)-2-oxo-ethyl]-2-[2-[2-[bis[2-(acetoxymethoxy)-2-oxo-ethyl]amino]phenoxy]ethoxy]anilino]acetate, with the chemical formula C2H4O, exhibits intriguing solubility characteristics that can be influenced by various factors:

  • Polarity: The presence of multiple acetoxymethoxy groups in the structure contributes to its polarity, making it potentially soluble in polar solvents.
  • Hydrogen Bonding: The functional groups capable of forming hydrogen bonds may enhance solubility in protic solvents like water.
  • Temperature Effects: Generally, the solubility of organic compounds can increase with temperature. This compound may follow that trend.
  • pH Dependence: The solubility can also vary significantly with pH; under acidic conditions, protonation can increase solubility due to ionic interactions.

In essence, this compound's solubility is governed by its complex molecular structure and interaction with the solvent environment. Understanding these parameters is critical for its applications and potential use in various fields.

Interesting facts

Exploring Acetoxymethyl 2-[N-[2-(acetoxymethoxy)-2-oxo-ethyl]-2-[2-[2-[bis[2-(acetoxymethoxy)-2-oxo-ethyl]amino]phenoxy]ethoxy]anilino]acetate

Acetoxymethyl 2-[N-[2-(acetoxymethoxy)-2-oxo-ethyl]-2-[2-[2-[bis[2-(acetoxymethoxy)-2-oxo-ethyl]amino]phenoxy]ethoxy]anilino]acetate is a complex organic compound that showcases the beauty and intricacy of molecular architecture. From a scientific perspective, this compound is particularly fascinating due to several key features:

  • Structural Complexity: The elaborate structure consists of multiple functional groups that signal its potential reactivity and versatility in various chemical reactions.
  • Biological Relevance: Compounds that include acetoxymethyl groups are often linked to pharmacological applications, acting as intermediates in the synthesis of pharmaceuticals.
  • Potential Applications: With its unique combination of moieties, this compound may play a role in drug development, especially in targeting specific biochemical pathways, or as a biochemical probe in research.
  • Research Significance: The study of such compounds can contribute to the understanding of structure-activity relationships (SAR) in medicinal chemistry, paving the way for the design of more effective therapeutic agents.

Furthermore, one of the remarkable aspects of studying complex compounds like this one is the interplay between chemistry and technology, as researchers continuously explore new methods to synthesize and manipulate such compounds for innovative solutions in various fields, including medicine, materials science, and environmental chemistry.

In conclusion, the unique attributes of Acetoxymethyl 2-[N-[2-(acetoxymethoxy)-2-oxo-ethyl]-2-[2-[2-[bis[2-(acetoxymethoxy)-2-oxo-ethyl]amino]phenoxy]ethoxy]anilino]acetate not only emphasize the creativity inherent in chemical synthesis but also highlight the potential these molecules have to inspire future scientific advancements.

Synonyms
BAPTA-AM
126150-97-8
acetyloxymethyl 2-[N-[2-(acetyloxymethoxy)-2-oxoethyl]-2-[2-[2-[bis[2-(acetyloxymethoxy)-2-oxoethyl]amino]phenoxy]ethoxy]anilino]acetate
MFCD00036696
BAPTA/AM
Glycine, N,N'-[1,2-ethanediylbis(oxy-2,1-phenylene)]bis[N-[2-[(acetyloxy)methoxy]-2-oxoethyl]-, 1,1'-bis[(acetyloxy)methyl] ester
(acetyloxy)methyl 2-({2-[(acetyloxy)methoxy]-2-oxoethyl}[2-(2-{2-[bis({2-[(acetyloxy)methoxy]-2-oxoethyl})amino]phenoxy}ethoxy)phenyl]amino)acetate
Tetrakis(acetoxymethyl) 1,2-Bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetate
Tetrakis(acetoxymethyl) 1,2-Bis(2-aminophenoxy)ethane-N,N,N,N-tetraacetate
Tetrakis(acetoxymethyl) 2,2',2'',2'''-(((ethane-1,2-diylbis(oxy))bis(2,1-phenylene))bis(azanetriyl))tetraacetate
Bio1_000382
Glycine, N,N'-[1,2-ethanediylbis(oxy-2,1-phenylene)]bis[N-[2-[(acetyloxy)methoxy]-2-oxoethyl]-, 1,1'-bis[(acetyloxy)methyl] ester; Glycine, N,N'-[1,2-ethanediylbis(oxy-2,1-phenylene)]bis[N-[2-[(acetyloxy)methoxy]-2-oxoethyl]-, bis[(acetyloxy)methyl] ester (9CI); BAPTA-AM
C34H40N2O18
1,2-Bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid tetrakis(acetoxymethyl ester)
BAPTA,AM
BAPTA Acetoxymethyl ester
BAPTA/AM(BAPTA-AM)
BAPTA/AM(BAPTA-AM)?
BSPBio_001472
SCHEMBL560577
CHEMBL1608767
CHEBI:92721
DTXSID60274361
YJIYWYAMZFVECX-UHFFFAOYSA-N
Bio1_000871
Bio1_001360
HMS3402J14
HMS3653N13
BCP06681
HB0981
s7534
AKOS015916296
BAPTA-AM, >=95% (HPLC)
CCG-270447
CS-7684
NCGC00163427-01
NCGC00163427-02
AS-75154
HY-100545
SW219561-1
T2845
BAPTA/AM - CAS 126150-97-8
A11437
BRD-K40919711-001-02-4
Q27164448
1,2-Bis(2-aminophenoxy)ethane-N,N,N ',N'-tetraacetic acid tetrakis(acetoxymethyl ester)
1,2-Bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic Acid Tetrakis(acetoxymethyl) Ester
2-[N-[2-(acetyloxymethoxy)-2-oxoethyl]-2-[2-[2-[bis[2-(acetyloxymethoxy)-2-oxoethyl]amino]phenoxy]ethoxy]anilino]acetic acid acetyloxymethyl ester