Page last updated: 2024-11-05

1,3-dithiane

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

Description

1,3-Dithiane is a cyclic organic compound with the formula (CH2)2S2. It is a white solid with a characteristic sulfurous odor. 1,3-Dithiane is used as a protecting group in organic synthesis, particularly for aldehydes and ketones. It can be readily synthesized from the reaction of 1,3-propanedithiol with an aldehyde or ketone in the presence of an acid catalyst. The resulting 1,3-dithiane derivative is stable and can be deprotected under mild conditions using mercury(II) chloride or Raney nickel. 1,3-Dithiane is also a useful reagent for the formation of carbon-carbon bonds, such as the Corey-Seebach reaction, in which a lithium derivative of 1,3-dithiane is used to add a carbon chain to an electrophile. 1,3-Dithiane is studied extensively in organic chemistry because of its versatile reactivity and its ability to protect carbonyl groups. Its synthetic versatility has led to its widespread use in the synthesis of complex organic molecules, including pharmaceuticals and natural products.'

1,3-dithiane: structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID10451
CHEBI ID47845
SCHEMBL ID27723
MeSH IDM0060326

Synonyms (40)

Synonym
c4h8s2
[1,3]dithiane
einecs 208-006-7
ai3-62288
nsc 157830
ccris 6777
dithiane-1,3 [french]
inchi=1/c4h8s2/c1-2-5-4-6-3-1/h1-4h
nsc-157830
m-dithiane
1,3-dithiane
nsc157830
505-23-7
1,3-dithiane, 97%
dithiane-1,3
CHEBI:47845
1,3-dithian
1,3-dithiacyclohexane
D0119
A828148
63527n060g ,
unii-63527n060g
FT-0606727
S10678
AKOS015856616
SCHEMBL27723
W-105954
mfcd00006654
DTXSID40198516
CS-W001189
1,3 dithiocyclohexane
m-dithiane, 8ci
AS-54491
SY014110
Q27120823
1.3-dithiane
HY-W001189
PB47614
EN300-97695
PD158227

Research Excerpts

Compound-Compound Interactions

ExcerptReferenceRelevance
"We report the use of 1,3-dithiane combined with aryldiazonium cation for the immobilization of biomolecules based on electrochemical addressing."( Use of 1,3-dithiane combined with aryldiazonium cation for immobilization of biomolecules based on electrochemical addressing.
Choi, SY; Haque, AM; Hong, JD; Kim, K; Kim, TH; Kwon, SR; Oh, YS; Park, H, 2009
)
1.13
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
dithiane
[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 (21)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (4.76)18.7374
1990's1 (4.76)18.2507
2000's4 (19.05)29.6817
2010's13 (61.90)24.3611
2020's2 (9.52)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 46.71

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 Index46.71 (24.57)
Research Supply Index3.09 (2.92)
Research Growth Index5.25 (4.65)
Search Engine Demand Index65.35 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (46.71)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other21 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]