Page last updated: 2024-12-08

trimethylsilyldiazomethane

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

Description

trimethylsilyldiazomethane: reagent for organic synthesis [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID167693
MeSH IDM0166983

Synonyms (67)

Synonym
trimethylsilyldiazomethane
AKOS015833333
diazomethyl-trimethyl-silane
FT-0657646
18107-18-1
T1146
tms-diazomethane
diazomethyl(trimethyl)silane
(trimethylsilyl)diazomethane
A812587
(diazomethyl)trimethylsilane
diazo((trimethylsilyl))methane
diazomethyltrimethyl silane
tmsd
hsdb 8011
qi98hqo8c4 ,
unii-qi98hqo8c4
tmschn2
silane, (diazomethyl)trimethyl-
S19225
diazo((trimethylsilyl))methane [hsdb]
trimethysilyl diazomethane
(trimethyl-silyl)diazomethane
diazomethyltrimethylsilane
(trimethylsilyl)-diazomethane
diazomethyl trimethylsilane
trimethyl-silyl diazomethane
trimethylsilyldiazomethan
(ch3)3sichn2
tms diazomethane
tmsdiazomethane
tmsch2n2
trimethylsilyldiazo methane
(diazomethyl)-trimethylsilane
tms-chn2
tmsdiazo methane
trimethlsilyl diazomethane
trimethylsilyldiazo- methane
(diazomethyl)(trimethyl)silane
(trimethylsilyl)diazo-methane
(trimethysilyl)diazomethane
trimethylsilyldiazo-methane
tms -diazomethane
diazomethyltrimethyl-silane
me3sichn2
trimethylsilyidiazomethane
trimethysilyldiazomethane
(trimethylsilyl) diazomethane
trimethyl silyl diazomethane
trimethylsilyl diazomethane
trimethylsilyl-diazomethane
DTXSID8074653
F8889-7517
mfcd00053946
AT25589
(trimethylsilyl)diazomethane, 10% in hexane
Q1990988
AMY15608
trimethylsilyldiazomethane, 2 m in diethyl ether
trimethylsilyldiazomethane, 2m in hexane
trimethylsilyldiazomethane, 10% in hexane
EN300-74206
[(z)-diazomethyl]-trimethylsilane
[(e)-diazomethyl]-trimethylsilane
trimethylsilyldiazomethane, ca. 10% in hexane, ca. 0.6mol/l
AT38821
c4h10n2si

Research Excerpts

Toxicity

ExcerptReferenceRelevance
"Diazomethane is a highly explosive and toxic gas routinely employed for the quantitative and clean derivatization of phenols."( Trimethylsilyldiazomethane: a safe non-explosive, cost effective and less-toxic reagent for phenol derivatization in GC applications.
Luthe, G; Rautiainen, RH; Robertson, LW; van 't Erve, TJ, 2010
)
1.8

Dosage Studied

ExcerptRelevanceReference
" The inter and intra assay precision were demonstrated to be lower than 20% and the relative bias to be lower than 15% in the dosing range of concentrations."( Validation of a novel and rapid method for the simultaneous determination of some phenolic organohalogens in human serum by GC-MS.
Charlier, C; Dufour, P; Pirard, C, 2016
)
0.43
[information is derived through text-mining from research 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's2 (5.56)18.2507
2000's13 (36.11)29.6817
2010's19 (52.78)24.3611
2020's1 (2.78)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 38.65

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 Index38.65 (24.57)
Research Supply Index3.61 (2.92)
Research Growth Index5.23 (4.65)
Search Engine Demand Index50.99 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (38.65)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (2.78%)6.00%
Case Studies1 (2.78%)4.05%
Observational0 (0.00%)0.25%
Other34 (94.44%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]