Page last updated: 2024-12-06
3,4-dimethylbenzaldehyde
3,4-dimethylbenzaldehyde is an organic compound with the formula CH3C6H3(CH3)CHO. It is a colorless liquid with a pungent odor. It is used as an intermediate in the synthesis of various organic compounds, including pharmaceuticals, dyes, and fragrances. 3,4-dimethylbenzaldehyde is also used as a flavoring agent in foods and beverages. The compound is synthesized by the Friedel-Crafts acylation of toluene with acetyl chloride in the presence of a Lewis acid catalyst, such as aluminum chloride. The resulting product is then oxidized to the corresponding aldehyde using a suitable oxidizing agent, such as potassium permanganate. 3,4-dimethylbenzaldehyde is a known irritant and can cause skin and eye irritation. It is also a potential allergen. The compound is studied for its potential applications in various fields, such as organic synthesis, medicine, and cosmetics. Its reactivity and versatility make it a valuable starting material for the development of new and useful compounds.'
Cross-References
ID Source | ID |
PubMed CID | 22278 |
CHEMBL ID | 3187739 |
CHEBI ID | 167406 |
SCHEMBL ID | 98097 |
MeSH ID | M0453407 |
Synonyms (41)
Synonym |
EN300-22064 |
CHEBI:167406 |
benzaldehyde, 3,4-dimethyl- |
3,4-dimethylbenzaldehyde |
3,4-dimethylbenzaldehyde, 98% |
o-xylene-4-carboxaldehyde |
5973-71-7 |
D3334 |
inchi=1/c9h10o/c1-7-3-4-9(6-10)5-8(7)2/h3-6h,1-2h3 |
poqjhlbmlvthau-uhfffaoysa- |
A832442 |
3,4-dimethyl-benzaldehyde |
3 pound not4-dimethylbenzaldehyde |
dtxcid0021626 |
tox21_301638 |
NCGC00255646-01 |
cas-5973-71-7 |
dtxsid2041626 , |
unii-16g1j12arb |
ec 227-770-2 |
16g1j12arb , |
einecs 227-770-2 |
AKOS009075842 |
FT-0614367 |
PS-4693 |
4-formyl-o-xylene |
SCHEMBL98097 |
3,4-dimethyl benzaldehyde |
3,4 dimethyl benzaldehyde |
3,4-di-methylbenzaldehyde |
SY004808 |
mfcd00016612 |
Q-200344 |
CHEMBL3187739 |
AC-3245 |
AC-15539 |
BCP24427 |
STL185667 |
Q27251808 |
CS-W013376 |
Z147641440 |
Drug Classes (1)
Class | Description |
carbonyl compound | Any compound containing the carbonyl group, C=O. The term is commonly used in the restricted sense of aldehydes and ketones, although it actually includes carboxylic acids and derivatives. |
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] |
Research
Studies (6)
Timeframe | Studies, This Drug (%) | All Drugs % |
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 4 (66.67) | 29.6817 |
2010's | 2 (33.33) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Market Indicators
Research Demand Index: 29.61
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.
Metric | This Compound (vs All) |
---|
Research Demand Index | 29.61 (24.57) | Research Supply Index | 1.95 (2.92) | Research Growth Index | 4.37 (4.65) | Search Engine Demand Index | 34.37 (26.88) | Search Engine Supply Index | 2.00 (0.95) |
| |
Study Types
Publication Type | This drug (%) | All Drugs (%) |
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 6 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |