Page last updated: 2024-12-05

triethylborane

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

Description

Triethylborane is a colorless, flammable liquid with a pungent odor. It is a strong reducing agent and can be used as a catalyst in organic reactions. Triethylborane is commonly used as a component in controlled radical polymerization processes and in the production of borane reagents. It is an important reagent in organic synthesis, and has applications in the fields of materials science, pharmaceuticals, and energy. Its importance in research is due to its ability to mediate a wide range of reactions, including hydroboration, carbonylation, and polymerization. The study of triethylborane is important because it can provide insight into the mechanisms of these reactions and the development of new and improved catalysts for these processes. Triethylborane is synthesized by reacting triethylaluminum with trimethyl borate. '

triethylborane: used in the radical deuteration reaction of ribonucleoside derivatives [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID7357
MeSH IDM0213412

Synonyms (31)

Synonym
hsdb 897
boron ethyl
einecs 202-620-9
brn 1731462
boron triethyl
triethylboron
triethylborine
triethylborane
inchi=1/c6h15b/c1-4-7(5-2)6-3/h4-6h2,1-3h
borane, triethyl-
triethylborane, >=95%
FT-0655589
97-94-9
T1984
A845771
AKOS009156530
triethyl-borane
z3s980z4p3 ,
unii-z3s980z4p3
4-04-00-04359 (beilstein handbook reference)
triethylborane [mi]
triethylboran
et3b
triethyl borane
bet3
DTXSID2052653
(c2h5)3b
borethyl
mfcd00009022
Q421149
EN300-35961

Research Excerpts

Effects

ExcerptReferenceRelevance
"Triethylborane has the potential to induce radical reactions on solid support and the solid-phase radical reactions were achieved by using triethylborane as a radical initiator. "( [Development of solid-phase radical reactions using oxime ethers as a radical acceptor].
Miyabe, H, 2000
)
1.75
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (23)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (4.35)18.7374
1990's1 (4.35)18.2507
2000's12 (52.17)29.6817
2010's9 (39.13)24.3611
2020's0 (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: 48.09

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 Index48.09 (24.57)
Research Supply Index3.18 (2.92)
Research Growth Index5.17 (4.65)
Search Engine Demand Index69.29 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (48.09)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews3 (13.04%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other20 (86.96%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]