Compounds > trimethoxyvinylsilane
Page last updated: 2024-11-06

trimethoxyvinylsilane

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

Trimethoxyvinylsilane (TMVS) is an organosilicon compound with the formula Si(OCH3)3(CH=CH2). It is a colorless liquid that is used as a coupling agent and adhesion promoter in various applications. TMVS is synthesized by the reaction of vinylmagnesium chloride with trimethylchlorosilane. It is also used as a precursor to other organosilicon compounds, such as silanes and polymers. TMVS is known to have a number of interesting properties, such as its ability to hydrolyze to form silanol groups, which can then react with other molecules to form siloxane bonds. This property makes TMVS useful as a coupling agent, as it can bind different materials together. TMVS is also known to have good adhesion properties, which make it useful as an adhesion promoter. It is used in a variety of applications, such as in the production of adhesives, sealants, and coatings. TMVS is also used in the synthesis of various other organic and inorganic materials. TMVS is studied due to its diverse applications in various industries, including adhesives, sealants, coatings, and composites. Its ability to act as a coupling agent and adhesion promoter, coupled with its versatility as a precursor for other silicon-based compounds, makes it a valuable material in research and development.'

Cross-References

ID SourceID
PubMed CID76004
SCHEMBL ID22614
MeSH IDM0521851

Synonyms (58)

Synonym
silane, trimethoxyvinyl-
sz 6300
einecs 220-449-8
ethenyltrimethoxysilane
kbm 1003
a 171 (silane derivative)
vts-m
v 4917
a 171
brn 1099136
y 4302
vinyl trimethoxy silane
(trimethoxysilyl)ethene
AKOS008901344
trimethoxyvinylsilane
vinyltrimethoxysilane ,
vinyltrimethoxysilane, 97%
vinyltrimethoxysilane, 98%
trimethoxy(vinyl)silane
silane, ethenyltrimethoxy-
2768-02-7
ethenyl(trimethoxy)silane
FT-0655075
inchi=1/c5h12o3si/c1-5-9(6-2,7-3)8-4/h5h,1h2,2-4h3
nksjnehgwdzzqf-uhfffaoysa-
ethenyl-trimethoxysilane
V0042
tox21_202575
dtxcid509240
cas-2768-02-7
dtxsid2029240 ,
NCGC00260124-01
A819155
unii-0ziu135ues
0ziu135ues ,
ec 220-449-8
AM84870
S22025
(trimethoxysilyl)ethylene
vinyl trimethoxysilane
ch2=chsi(och3)3
(ch3o)3sich=ch2
SCHEMBL22614
dynasylan silfin
dynasylan vtmo
union carbide a-171
cv-4917
vtmo
mfcd00008605
J-016856
E75732
vinyl-trimethoxy-silane
(trimethoxysilyl)ethylene, ethenyltrimethoxysilane
AS-17409
vinyltrimethoxy-silane
Q27251076
trimethoxyvinylsilane 100 microg/ml in acetonitrile
EN300-7405193
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (1)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency32.98270.001530.607315,848.9004AID1224841
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (9)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (22.22)29.6817
2010's6 (66.67)24.3611
2020's1 (11.11)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 39.55

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 strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index39.55 (24.57)
Research Supply Index2.30 (2.92)
Research Growth Index4.72 (4.65)
Search Engine Demand Index54.33 (26.88)
Search Engine Supply Index2.13 (0.95)

This Compound (39.55)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies1 (11.11%)4.05%
Observational0 (0.00%)0.25%
Other8 (88.89%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
methanol
Methanol: A colorless, flammable liquid used in the manufacture of FORMALDEHYDE and ACETIC ACID, in chemical synthesis, antifreeze, and as a solvent. Ingestion of methanol is toxic and may cause blindness.. primary alcohol : A primary alcohol is a compound in which a hydroxy group, -OH, is attached to a saturated carbon atom which has either three hydrogen atoms attached to it or only one other carbon atom and two hydrogen atoms attached to it.. methanol : The primary alcohol that is the simplest aliphatic alcohol, comprising a methyl and an alcohol group.		2.0510alkyl alcohol;
one-carbon compound;
primary alcohol;
volatile organic compound		amphiprotic solvent;
Escherichia coli metabolite;
fuel;
human metabolite;
mouse metabolite;
Mycoplasma genitalium metabolite
azobis(isobutyronitrile)
azobis(isobutyronitrile): blowing agent for elastomers & plastics; initiator for free radical reactions; structure		2.0410
n-butyl acrylate
butyl acrylate : An acrylate ester obtained by the formal condensation of the hydroxy group of butan-1-ol with the carboxy group of acrylic acid.		2.0810acrylate ester
2,2,2-trifluoroethyl methacrylate
[no description available]		2.0810
tetramethoxysilane
[no description available]		2.4820
fluorescein
Fluorescein: A phthalic indicator dye that appears yellow-green in normal tear film and bright green in a more alkaline medium such as the aqueous humor.. fluorescein (lactone form) : A xanthene dye that is highly fluorescent, detectable even when present in minute quantities. Used forensically to detect traces of blood, in analytical chemistry as an indicator in silver nitrate titrations and in microscopy.		2.13102-benzofurans;
gamma-lactone;
organic heteropentacyclic compound;
oxaspiro compound;
polyphenol;
xanthene dye		fluorescent dye;
radioopaque medium
n-octadecyl mercaptan
n-octadecyl mercaptan: structure given in first source		2.1510
vinylphosphonic acid
[no description available]		2.1510
organophosphonates
hydrogenphosphite : A divalent inorganic anion resulting from the removal of a proton from two of the hydroxy groups of phosphorous acid.		2.1510divalent inorganic anion;
phosphite ion
calixarenes
Calixarenes: Phenolic metacyclophanes derived from condensation of PHENOLS and ALDEHYDES. The name derives from the vase-like molecular structures. A bracketed [n] indicates the number of aromatic rings.. calixarenes : Originally macrocyclic compounds capable of assuming a basket (or "calix") shaped conformation. They are formed from p-hydrocarbyl phenols and formaldehyde. The term now applies to a variety of derivatives by substitution of the hydrocarbon cyclo{oligo[(1,3-phenylene)methylene]}.. calixarene : A macrocycle composed of 1,3-phenylene groups linked by methylene groups. The number of 1,3-phenylene units in the macrocycle is denoted by the "n" in calix[n]arene name.		2.0410
3-mercapto-1-propanesulfonate
3-mercapto-1-propanesulfonate: structure in first source		2.1510
laponite
laponite: a synthesized hectorite; chemical formula in first source		2.1310
ConditionIndicatedRelationship StrengthStudiesTrials
Burns, Chemical
Burns caused by contact with or exposure to CAUSTICS or strong ACIDS.		02.0510