Page last updated: 2024-12-08

1-(chloromethyl)silatrane

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

Description

## 1-(Chloromethyl)silatrane: A Powerful Tool in Research

1-(Chloromethyl)silatrane, also known as **chloromethyltris(2-hydroxyethyl)silane**, is a versatile organosilicon compound with a unique structure. It consists of a central silicon atom surrounded by three 2-hydroxyethyl groups and a chloromethyl group. This molecule is particularly important for research due to its:

**1. Reactivity:** The chloromethyl group in 1-(chloromethyl)silatrane acts as a reactive site, allowing for the formation of diverse derivatives through various chemical transformations. These transformations include:

* **Nucleophilic Substitution:** The chlorine atom can be readily replaced by various nucleophiles, such as amines, alkoxides, and thiols. This allows for the synthesis of a wide range of functionalized silatranes with specific properties.
* **Ring-Opening Reactions:** The silatrane framework can be opened under specific conditions, providing access to new silicon-containing compounds with different functionalities.

**2. Biological Activity:** 1-(Chloromethyl)silatrane and its derivatives have shown promising biological activity, particularly in the following areas:

* **Antimicrobial Agents:** Some derivatives exhibit antimicrobial activity against bacteria, fungi, and even viruses.
* **Anticancer Agents:** Certain silatrane-based compounds demonstrate cytotoxic effects against specific cancer cell lines.
* **Bioimaging Probes:** The unique structure and reactivity of silatranes allow them to be functionalized with fluorescent groups, making them valuable tools for bioimaging and drug delivery applications.

**3. Material Science Applications:** 1-(Chloromethyl)silatrane and its derivatives have found applications in the development of advanced materials, including:

* **Polymers and Composites:** The reactive chloromethyl group can be used to incorporate silatranes into polymer chains, enhancing their mechanical properties and thermal stability.
* **Nanomaterials:** Silatranes can be utilized for the synthesis of novel nanomaterials with controlled size and morphology, leading to unique optical and electronic properties.

**4. Chemical Reactivity Studies:** 1-(Chloromethyl)silatrane serves as a valuable model compound for studying the reactivity of silatrane systems. Its unique structure and reactivity provide insights into the behavior of silicon in different chemical environments, contributing to the advancement of silicon chemistry.

**In summary:** 1-(Chloromethyl)silatrane's reactivity, biological activity, and material science applications make it a crucial compound in research. It serves as a versatile building block for synthesizing new functional molecules, offering valuable insights into the chemistry and biology of silicon-containing compounds.

Silimin: contains collagen, hydroxyapatite & CM-silitrane; Russian compound; a biogenic composite material for dental implants [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID362521
CHEMBL ID2000017
SCHEMBL ID8418895
MeSH IDM0104675

Synonyms (33)

Synonym
42003-39-4
AKOS005429972
nsc626545
nsc-626545
chloromethylsilatrane
2,8,9-trioxa-5-aza-1-silabicyclo[3.3.3]undecane, 1-(chloromethyl)-
5-(chloromethyl)-4,6,11-trioxa-1-aza-5-silabicyclo[3.3.3]undecane
1-(chloromethyl)-2,8,9-trioxa-5-aza-1-silabicyclo[3.3.3]undecane
NCI60_008397
1-chloromethyl-2,8,9-trioxa-5-aza-1-sila-bicyclo[3.3.3]undecane
STK363119
2,8,9-trioxa-5-aza-1-silabicyclo(3.3.3)undecane, 1-(chloromethyl)-
silimin
1-(chloromethyl)silatrane
mival
1-(chloromethyl)-2,8,9-trioxa-5-aza-1-silabicyclo(3.3.3)undecane
1-chloromethylsilatrane
einecs 255-621-1
BBL000525
unii-7r9b5a0vph
7r9b5a0vph ,
1-(chloromethyl)-2,8,9-trioxa-5-aza-1- silabicyclo(3.3.3)undecane
1-chloromethyl silatrane
chloromethylsilatrane [who-dd]
2,8,9-trioxa-5-aza-1-silabicyclo(3.3.3)undecane, 1- (chloromethyl)-
CHEMBL2000017
SCHEMBL8418895
DTXSID2041383
mfcd00053377
1-chloromethyl-2,8,9-trioxa-5-aza-1-sila-bicyclo(3.3.3)undecane
VS-00636
Q27268749
CS-0357933
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (15)

TimeframeStudies, This Drug (%)All Drugs %
pre-19907 (46.67)18.7374
1990's7 (46.67)18.2507
2000's1 (6.67)29.6817
2010's0 (0.00)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: 11.03

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

MetricThis Compound (vs All)
Research Demand Index11.03 (24.57)
Research Supply Index3.14 (2.92)
Research Growth Index4.17 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.03)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (4.76%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other20 (95.24%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]