Page last updated: 2024-12-05

methacrylaldehyde

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Cross-References

ID SourceID
PubMed CID6562
CHEMBL ID4063095
CHEBI ID88384
MeSH IDM0117433

Synonyms (63)

Synonym
wln: vhy1&u1
2-methylpropenal
2-methylenepropanal
2-methylacrolein
methacrylic aldehyde
acrolein, 2-methyl-
nsc8260
.alpha.-methylacrolein
methacrolein
.alpha.-methacrolein
methacrylaldehyde
methylacrylaldehyde
78-85-3
nsc-8260
isobutenal
2-propenal, 2-methyl-
2-methylpropenal [czech]
un2396
ai3-37779
2-methyl-2-propenal
nsc 8260
hsdb 182
methakrylaldehyd [czech]
brn 1209258
alpha-methylacrolein
ccris 1153
einecs 201-150-1
2-methylacrylaldehyde
inchi=1/c4h6o/c1-4(2)3-5/h3h,1h2,2h
methacrolein, 95%
2-methylprop-2-enal
M0078
AKOS000119839
A839511
FT-0671115
4-01-00-03455 (beilstein handbook reference)
unii-9hrb24892h
methakrylaldehyd
methacrylaldehyde, inhibited
methacrylaldehyde, inhibited [un2396] [flammable liquid]
9hrb24892h ,
FT-0628270
2-formyl-1-propene
methacrolein [hsdb]
.alpha.-methylacrylaldehyde
methacryaldehyde
methacroleine
2-methyl-propenal
DTXSID0052540
ch2=c(ch3)cho
methacraldehyde
un 2396 (salt/mix)
2-methylacrylaldehyde #
F2191-0163
mfcd00006974
CHEBI:88384
H10713
methacrolein (stabilized with hq)
Q420234
AMY28760
CHEMBL4063095
methacrolein (stabilized with 1per cent hydroquinone)
EN300-19749
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
enalAn alpha,beta-unsaturated aldehyde of general formula R(1)R(2)C=CR(3)-CH=O in which the aldehydic C=O function is conjugated to a C=C double bond at the alpha,beta position.
[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]

Bioassays (1)

Assay IDTitleYearJournalArticle
AID1469819Glutathione reactivity of the compound in DMSO and phosphate buffer assessed as second order rate constant for adduct formation2017Journal of medicinal chemistry, 02-09, Volume: 60, Issue:3
Covalent Modifiers: A Chemical Perspective on the Reactivity of α,β-Unsaturated Carbonyls with Thiols via Hetero-Michael Addition Reactions.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (36)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (2.78)18.7374
1990's1 (2.78)18.2507
2000's9 (25.00)29.6817
2010's19 (52.78)24.3611
2020's6 (16.67)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 22.23

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.

MetricThis Compound (vs All)
Research Demand Index22.23 (24.57)
Research Supply Index3.64 (2.92)
Research Growth Index5.28 (4.65)
Search Engine Demand Index21.17 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (22.23)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (2.78%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other35 (97.22%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]