Interesting facts
1,3-Dimethoxybenzene: A Unique Aromatic Compound
1,3-Dimethoxybenzene, commonly known as m-Dimethoxybenzene or m-Anisole, is an interesting compound in the field of organic chemistry. As a member of the class of aromatic hydrocarbons, it features a distinct structure that contributes to its unique properties and applications. Here are some captivating facts about this compound:
- Aromaticity: This compound contains a benzene ring substituent, which imparts notable stability and unique reactivity.
- Substituents: The presence of two methoxy groups (-OCH3) in the 1 and 3 positions is responsible for influencing the electronic properties of the compound, often increasing its nucleophilic character.
- Applications: 1,3-Dimethoxybenzene is used in a variety of applications, including:
- Synthesis of pharmaceuticals
- Manufacture of fragrances and flavors
- As a precursor in the production of agrochemicals
- Reactivity: The compound participates in electrophilic aromatic substitution reactions, making it an important factor in synthetic organic chemistry.
- Performance in Research: Various studies have indicated that compounds like 1,3-dimethoxybenzene can be investigated for their effects in biological systems, including potential antioxidant properties.
In conclusion, 1,3-dimethoxybenzene is more than just a simple aromatic compound. Its unique structure and versatile reactivity make it a notable subject of research within the realms of organic synthesis and industrial applications. The exploration of such compounds opens up significant avenues for scientific advancements and innovative applications in multiple fields.
Synonyms
1,3-Dimethoxybenzene
151-10-0
Benzene, 1,3-dimethoxy-
M-DIMETHOXYBENZENE
Resorcinol dimethyl ether
3-Methoxyanisole
Benzene, m-dimethoxy-
Dimethyl resorcinol
Methoxyanisole, m-
m-Methoxyanisole
Dimethylresorcinol
Dimethylether resorcinolu
FEMA No. 2385
m-dimethoxy-benzene
m-Dimethoxy benzene
1,3-DIMETHOXY BENZENE
Dimethylether resorcinolu [Czech]
NSC 8699
EINECS 205-783-4
UNII-2694Z07HQY
DTXSID2047060
AI3-00845
1,3-Dimethoxy-benzene
2694Z07HQY
NSC-8699
meta-dimethyl hydroquinone
1,3-DIMETHOXYBENZEN-2,4,5,6-D4
DTXCID0027060
CHEBI:89853
M-DIMETHOXYBENZENE [FHFI]
3-METHOXYPHENYL METHYL ETHER
mMethoxyanisole
3Methoxyanisole
mDimethoxybenzene
Methoxyanisole, m
Benzene, mdimethoxy
meta-dimethoxybenzene
MFCD00008384
1,3 dimethoxybenzene
Benzene,3-dimethoxy-
resorcinol dimethylether
Benzene, 1,3dimethoxy
SCHEMBL9350
CHEMBL2252486
SCHEMBL13322163
1,3-Dimethoxybenzene, >=98%
NSC8699
STR00616
Tox21_302348
1,3-Dimethoxybenzene, >=98%, FG
AKOS000120162
CS-W018510
FD02251
NCGC00256016-01
1,3-Dimethoxybenzene, analytical standard
CAS-151-10-0
HY-34487
DB-013763
D0628
NS00013171
EN300-16149
Resorcinol dimethyl ether;2,4-Dimethoxybenzene
Q27162036
F0001-0538
205-783-4
Solubility of 1,3-Dimethoxybenzene
1,3-Dimethoxybenzene, also known as methylene dimethyl ether, exhibits unique solubility properties that are noteworthy. Here are some key points regarding its solubility:
In summary, while 1,3-dimethoxybenzene is not particularly soluble in water, its solubility in organic solvents opens doors to a wide range of chemical applications. Understanding these solubility properties is crucial for effective utilization in both laboratory settings and industrial applications.