Interesting facts
Interesting Facts About 4-Methoxybenzaldehyde
4-Methoxybenzaldehyde, also known as para-methoxybenzaldehyde, is an organic compound with significant relevance in various fields of chemistry. Here are some intriguing aspects of this compound:
- Structure and Characteristics: 4-Methoxybenzaldehyde features a methoxy group (-OCH3) attached to the benzaldehyde structure. This slight modification influences its reactivity and properties, setting it apart from other aldehydes.
- Applications: This compound is widely utilized in organic synthesis and serves as a precursor in the production of fragrances and flavoring agents. It is particularly valued in the creation of floral and sweet aromas.
- As a Building Block: Chemists often use 4-methoxybenzaldehyde as a versatile building block in the synthesis of pharmaceuticals and agrochemicals. Its derivatives are important in developing compounds that exhibit biological activity.
- Reactivity: Like many aldehydes, 4-methoxybenzaldehyde readily undergoes oxidation to carboxylic acids. This property makes it useful in a range of chemical reactions, including aldol reactions and condensation reactions.
- Research Insights: Studies have shown that compounds bearing the methoxy group can exhibit unique biological properties. Research is ongoing to explore its potential applications in drug design and development.
- Historical Significance: The compound is often mentioned in historical contexts regarding the development of organic chemistry. The methodologies used to synthesize and manipulate 4-methoxybenzaldehyde have paved the way for modern synthetic techniques.
As chemists continue to explore this fascinating compound, it serves as a reminder of the intricate connections between structure, reactivity, and application in the world of chemistry. With its diverse functionalities, 4-methoxybenzaldehyde exemplifies the beauty and complexity of organic compounds.
Synonyms
4-Methoxybenzaldehyde
123-11-5
P-ANISALDEHYDE
Anisaldehyde
p-Methoxybenzaldehyde
Benzaldehyde, 4-methoxy-
4-Anisaldehyde
p-Formylanisole
Crategine
Obepin
p-Anisic aldehyde
para-anisaldehyde
4-Methoxy-benzaldehyde
FEMA No. 2670
DTXSID2026997
9PA5V6656V
NSC-5590
DTXCID906997
CHEBI:28235
RefChem:44849
204-602-6
256-891-3
Anisic aldehyde
Aubepine
MFCD00003385
4-methoxy benzaldehyde
anisal
NSC 5590
p-methoxy benzaldehyde
para-methoxybenzaldehyde
50984-52-6
p-Methoxybenzaldehyde-13C6
CHEMBL161598
Formylanisole, p-
Caswell No. 051E
CAS-123-11-5
CCRIS 821
p-Methoxybenzaldehyde (natural)
HSDB 2641
EINECS 204-602-6
anisaldehyd
Anis aldehyde
UNII-9PA5V6656V
AI3-00223
FEMA 2670
4-methoxybenzaldehye
4-methoxybezaldehyde
EINECS 256-891-3
Anisaldehyde (para)
4-methoxylbenzaldehyde
p-Anisaldehyde, 8CI
4-methoxybenzylaldehyde
BRN 0471382
p-Anisaldehyde, 98%
p-Anisaldehyde, Reagent
para-methoxy benzaldehyde
benzaldehyde, p-methoxy-
4-(methyloxy)benzaldehyde
bmse010130
WLN: VHR DO1
EC 204-602-6
SCHEMBL1099
SCHEMBL1100
P-ANISALDEHYDE [MI]
68894-36-0
MLS002152921
P-ANISALDEHYDE [HSDB]
p-Methoxybenzylidenemalonitrile
4-methoxybenzene carboxaldehyde
orb1299391
SCHEMBL1205513
SCHEMBL1206990
SCHEMBL7289096
PARA- METHOXYBENZALDEHYDE
P-ANISALDEHYDE [USP-RS]
HY-Y0740R
4-Methoxybenzaldehyde (Standard)
NSC5590
HMS3039F08
HMS5084L03
p-Anisaldehyde, analytical standard
P-METHOXYBENZALDEHYDE [FCC]
HY-Y0740
PXB44155
p-Anisaldehyde, natural, 98%, FG
P-METHOXYBENZALDEHYDE [FHFI]
Tox21_201943
Tox21_303331
AC7808
BDBM50139370
MSK014067
s5086
SBB040224
STL194068
AKOS000118814
CCG-214805
CS-W020189
FM05674
p-Anisaldehyde (4-Methoxybenzaldehyde)
p-Anisaldehyde, for synthesis, 98.0%
NCGC00090807-01
NCGC00090807-02
NCGC00257076-01
NCGC00259492-01
p-Anisaldehyde, >=97.5%, FCC, FG
AC-10379
BP-14175
CS-11005
SMR001224521
SY001689
DB-012818
A0480
A1674
BENZALDEHYDE,4-METHOXY MFC8 H8 O2
NS00003331
ST50213373
EN300-16096
4-08-00-00252 (Beilstein Handbook Reference)
A805017
F079445
Q174937
doi:10.14272/ZRSNZINYAWTAHE-UHFFFAOYSA-N.1
doi:10.14272/ZRSNZINYAWTAHE-UHFFFAOYSA-N.2
MEPYRAMINE MALEATE IMPURITY P [EP IMPURITY]
Z53833125
F2190-0575
p-Anisaldehyde, primary pharmaceutical reference standard
p-Anisaldehyde, certified reference material, TraceCERT(R)
p-Anisaldehyde, United States Pharmacopeia (USP) Reference Standard
InChI=1/C8H8O2/c1-10-8-4-2-7(6-9)3-5-8/h2-6H,1H
Solubility of 4-methoxybenzaldehyde
4-methoxybenzaldehyde, with the chemical formula C8H8O2, exhibits interesting solubility characteristics that are influenced by its molecular structure. This organic compound, also known as p-anisaldehyde, is known for its aromatic properties and moderate polarity.
When it comes to solubility in various solvents, 4-methoxybenzaldehyde can be summarized as follows:
To sum up, the solubility of 4-methoxybenzaldehyde is a reflection of its chemical nature, where it favors solubility in organic environments rather than in aqueous solutions. The ability to dissolve in organic solvents makes this compound particularly useful for various applications in organic synthesis.