Silane,(3-azidopropyl)triethoxy-
- CasNo:83315-69-9
Product Description
Factory supply Silane,(3-azidopropyl)triethoxy- 83315-69-9 with sufficient stock and high standard
- Molecular Formula: C9H21N3O3Si
- Molecular Weight: 247.37
83315-69-9 Relevant articles
Covalent immobilization of aggregation-induced emission luminogens in silica nanoparticles through click reaction
Mahtab, Faisal,Lam, Jacky W. Y.,Yu, Yong,Liu, Jianzhao,Yuan, Wangzhang,Lu, Ping,Tang, Ben Zhong
, p. 1448 - 1455 (2011)
Fluorescent silica nanoparticles (FSNPs)...
Silicium dioxide nanoparticles as carriers for photoactivatable co-releasing molecules (PhotoCORMs)
Doerdelmann, Gregor,Pfeiffer, Hendrik,Birkner, Alexander,Schatzschneider, Ulrich
, p. 4362 - 4367 (2011)
Silicium dioxide nanoparticles of about ...
Highly active enzymes immobilized in large pore colloidal mesoporous silica nanoparticles
G??l, Dorothée,Singer, Helena,Chiu, Hsin-Yi,Schmidt, Alexandra,Lichtnecker, Martina,Engelke, Hanna,Bein, Thomas
, p. 1671 - 1680 (2019)
Various bio-applications of mesoporous m...
An original "click and bind" approach for immobilizing copper hexacyanoferrate nanoparticles on mesoporous silica
Turgis, Raphael,Arrachart, Guilhem,Delchet, Carole,Rey, Cyrielle,Barre, Yves,Pellet-Rostaing, Stephane,Guari, Yannick,Larionova, Joulia,Grandjean, Agnes
, p. 4447 - 4453 (2013)
We present an original approach for prep...
Synthesis, characterization and structural aspects of 3- azidopropylsilatrane
Singh, Raghubir,Puri, Jugal Kishore,Pal Sharma, Raj,Kumar Malik, Ashok,Ferretti, Valeria
, p. 107 - 112 (2010)
Reaction of 3-chloropropyltriethoxysilan...
Click chemistry: A new facile and efficient strategy for preparation of functionalized HPLC packings
Guo, Zhimou,Lei, Aiwen,Liang, Xinmiao,Xu, Qing
, p. 4512 - 4514 (2006)
Click chemistry has been successfully ex...
CB[8]-based rotaxane as a useful platform for sensitive detection and discrimination of explosives
Zhu, Wei,Li, Weina,Wang, Chen,Cui, Jiecheng,Yang, Haowei,Jiang, Yin,Li, Guangtao
, p. 3583 - 3590 (2013)
Based on a naphthalene-threaded cucurbit...
A new heterogeneous host-guest catalytic system as an eco-friendly approach for the synthesis of cyclic carbonates from CO2 and epoxides
Mirabaud, Ana?s,Martinez, Alexandre,Bayard, Fran?ois,Dutasta, Jean-Pierre,Dufaud, Véronique
, p. 16863 - 16874 (2018)
Two strategies have been explored toward...
Synthesis of glyco-silicas by Cu(I)-catalyzed "click-chemistry" and their applications in affinity chromatography
Ortega-Munoz, Mariano,Lopez-Jaramillo, Javier,Hernandez-Mateo, Fernando,Santoyo-Gonzalez, Francisco
, p. 2410 - 2420 (2006)
The covalent immobilization of suitable ...
Hg2+ wettability and fluorescence dual-signal responsive switch based on a cysteine complex of piperidine-calix[4]arene
Zhang, Xiaoyan,Zhao, Haiyang,Cao, Xianliang,Feng, Ningmei,Tian, Demei,Li, Haibing
, p. 8262 - 8268 (2013)
The recognition of the mercury(ii) ion (...
Triazole/Triazine-Functionalized Mesoporous Silica As a Hybrid Material Support for Palladium Nanocatalyst
Saad, Ali,Vard, Christian,Abderrabba, Manef,Chehimi, Mohamed M.
, p. 7137 - 7146 (2017)
Noble and precious metal catalysts are s...
Facile route to functionalized mesoporous silica nanoparticles by click chemistry
Moitra, Nirmalya,Trens, Philippe,Raehm, Laurence,Durand, Jean-Olivier,Cattoen, Xavier,Chi Man, Michel Wong
, p. 13476 - 13482 (2011)
Mesoporous silica nanoparticles containi...
First report of silver ion recognition via a silatrane-based receptor: excellent selectivity, low detection limit and good applicability
Singh, Gurjaspreet,Singh, Akshpreet,Satija, Pinky,Sharma, Geetika,Shilpy,Singh, Jandeep,Singh, Jasbhinder,Singh, Kamal Nain,Kaur, Amarjit
, p. 5525 - 5530 (2019)
The development of selective and sensiti...
Fabrication of functional waterborne polyurethane/montmorillonite composites by click chemistry method
Sun, Daoxing,Li, Rong,Li, Xingjian,Wang, Wenjuan,Hu, Jing
, p. 522 - 528 (2012)
"Click" chemistry method was used to fab...
Facile syntheses of alkoxysilanated phosphorylcholines as surface modifiers: CuAAC and thiol-ene "click" reactions
Liu, Lei,Park, Sung Jin,Park, Ji-Hyun,Lee, Myong Euy
, p. 14273 - 14276 (2015)
Eight alkoxysilanated phosphorylcholine ...
Designing of thiosemicarbazone-triazole linked organotriethoxysilane as UV-Visible and fluorescence sensor for the selective detection of Hg2+ ions and their cytotoxic evaluation
Angeles Esteban, Maria,Diksha,Espinosa-Ruíz, Cristóbal,González-Silvera, D.,Gupta, Sofia,Mohit,Priyanka,Singh, Gurjaspreet,Sushma
, (2022/02/02)
In this manuscript, a new series of thio...
Heterogeneous Fe3O4@Si–NHC–Pd Catalyst: Synthesis, Characterization, and Catalytic Activity in the Suzuki–Miyaura Cross-Coupling Reaction under Mild Conditions
Kalishomi, R. Ghavidel,Rostamizadeh, S.
, p. 1140 - 1146 (2021/08/06)
Abstract: A novel Fe3O4@Si–NHC–Pd cataly...
Multi-stimuli Photo and Redox-active Nanostructured Mesoporous Silica Films on Transparent Electrodes
Ahoulou, Samuel,Vilà, Neus,Pillet, Sébastien,Carteret, Cédric,Schaniel, Dominik,Walcarius, Alain
, p. 2464 - 2477 (2021/10/30)
Silica matrices hosting transition metal...
LIGHT TRIGGERABLE GENE EDITING FORMULATION, IN VIVO EDITING METHOD, AND USES THEREOF
-
Paragraph 0084, (2020/12/07)
The disclosure comprises a formulation c...
83315-69-9 Process route
-
-
5089-70-3
(3-chloropropyl)triethoxysilane
-
-
83315-69-9
3-azidopropyltriethoxysilane
| Conditions | Yield |
|---|---|
|
With
Caswell No. 744A;
In
butanone;
for 72h;
Inert atmosphere;
Reflux;
|
96%
|
|
With
Caswell No. 744A;
In
dimethyl sulfoxide;
at 60 ℃;
|
95%
|
|
With
Caswell No. 744A; tetrabutylammonium bromide;
In
acetonitrile;
for 20h;
Reflux;
Inert atmosphere;
|
95%
|
|
With
Caswell No. 744A;
In
N,N-dimethyl-formamide;
at 120 ℃;
for 24h;
|
92%
|
|
With
Caswell No. 744A;
In
N,N-dimethyl-formamide;
at 90 ℃;
for 4h;
|
91%
|
|
With
Caswell No. 744A;
In
N,N-dimethyl-formamide;
at 90 ℃;
for 4h;
|
91%
|
|
With
Caswell No. 744A; butyrylaldehyde;
for 72h;
Reflux;
|
90%
|
|
With
Caswell No. 744A;
In
N,N-dimethyl-formamide;
at 90 ℃;
for 6h;
|
90%
|
|
With
Caswell No. 744A;
In
N,N-dimethyl-formamide;
at 90 ℃;
for 4h;
Inert atmosphere;
|
89%
|
|
With
Caswell No. 744A;
In
N,N-dimethyl-formamide;
at 90 ℃;
for 4h;
Inert atmosphere;
Schlenk technique;
|
89%
|
|
With
Caswell No. 744A; tetrabutylammonium bromide;
In
acetonitrile;
for 48h;
Inert atmosphere;
Reflux;
|
82%
|
|
With
Caswell No. 744A; tetrabutylammonium bromide;
In
acetonitrile;
for 24h;
Inert atmosphere;
Reflux;
|
81%
|
|
With
Caswell No. 744A; tetrabutylammonium bromide;
In
acetonitrile;
for 48h;
Reflux;
Inert atmosphere;
|
80%
|
|
With
Caswell No. 744A; N,N,N-tributyl-1-butanaminium iodide;
In
butanone;
for 120h;
Reflux;
Inert atmosphere;
|
80%
|
|
With
Caswell No. 744A; tetra-n-butylammonium azide;
In
acetonitrile;
for 70h;
Reflux;
|
76%
|
|
With
Caswell No. 744A; tetrabutylammonium bromide;
In
acetonitrile;
for 18h;
Inert atmosphere;
Reflux;
|
74%
|
|
With
Caswell No. 744A; tetrabutylammonium bromide;
In
acetonitrile;
for 18h;
Inert atmosphere;
Reflux;
|
74%
|
|
With
Caswell No. 744A; sodium iodide;
In
dimethyl sulfoxide;
at 60 ℃;
for 18h;
Schlenk technique;
Inert atmosphere;
|
74%
|
|
With
Caswell No. 744A;
In
N,N-dimethyl-formamide;
at 90 ℃;
for 5h;
Inert atmosphere;
|
68%
|
|
With
Caswell No. 744A;
In
N,N-dimethyl-formamide;
at 90 ℃;
for 4h;
Inert atmosphere;
|
64%
|
|
With
Caswell No. 744A;
In
N,N-dimethyl-formamide;
at 90 ℃;
for 4h;
Inert atmosphere;
|
64%
|
|
With
Caswell No. 744A; tetrabutylammonium bromide;
In
acetonitrile;
at 90 ℃;
for 18h;
Inert atmosphere;
|
60%
|
|
With
Caswell No. 744A; tetrabutylammonium bromide;
In
acetonitrile;
for 18h;
Inert atmosphere;
Reflux;
|
60%
|
|
With
Caswell No. 744A; sodium iodide;
In
dimethyl sulfoxide;
at 60 ℃;
for 24h;
Inert atmosphere;
|
41%
|
|
With
Caswell No. 744A; N,N,N-tributyl-1-butanaminium iodide;
In
butanone;
for 50h;
Heating;
|
|
|
With
Caswell No. 744A; potassium iodide;
In
N,N-dimethyl-formamide;
at 90 - 100 ℃;
|
|
|
With
Caswell No. 744A; sodium iodide;
In
toluene;
at 70 - 80 ℃;
|
|
|
Multi-step reaction
with
2
steps
1: sodium iodide / acetone / 72 h / Reflux; Inert atmosphere
2: Caswell No.
744A / N,N-dimethyl-formamide / 72 h / 50 °C / Inert atmosphere
With
Caswell No. 744A; sodium iodide;
In
N,N-dimethyl-formamide; acetone;
|
|
|
With
Caswell No. 744A; tetrabutylammonium bromide;
In
acetonitrile;
Reflux;
|
|
|
With
Caswell No. 744A; tetrabutylammonium bromide;
In
acetonitrile;
for 18h;
Reflux;
Inert atmosphere;
|
|
|
With
Caswell No. 744A;
|
|
|
With
Caswell No. 744A;
In
N,N-dimethyl-formamide;
at 90 ℃;
for 8h;
Inert atmosphere;
|
|
|
With
Caswell No. 744A;
In
N,N-dimethyl-formamide;
at 90 ℃;
for 4h;
Inert atmosphere;
|
|
|
With
Caswell No. 744A;
In
N,N-dimethyl-formamide;
at 80 ℃;
for 4h;
Inert atmosphere;
|
|
|
With
Caswell No. 744A;
In
acetonitrile;
for 20h;
Reflux;
|
|
|
Multi-step reaction
with
2
steps
1: sodium iodide / acetone / 72 h / Reflux
2: Caswell No.
744A / N,N-dimethyl-formamide / 72 h / 50 °C
With
Caswell No. 744A; sodium iodide;
In
N,N-dimethyl-formamide; acetone;
|
|
|
With
Caswell No. 744A;
|
|
|
With
Caswell No. 744A;
In
N,N-dimethyl-formamide;
at 90 ℃;
for 4h;
Inert atmosphere;
|
|
|
With
Caswell No. 744A;
In
N,N-dimethyl-formamide;
at 70 - 100 ℃;
|
|
|
With
Caswell No. 744A;
In
N,N-dimethyl-formamide;
at 90 ℃;
for 4h;
|
|
|
With
Caswell No. 744A;
In
N,N-dimethyl-formamide;
at 90 ℃;
for 4h;
|
|
|
With
Caswell No. 744A; N-hexadecyl-N,N,N-trimethylammonium bromide;
In
acetonitrile;
for 48h;
Inert atmosphere;
Reflux;
|
|
|
With
Caswell No. 744A; tetra-n-hexylammonium bromide;
In
acetonitrile;
at 82 ℃;
for 18h;
Inert atmosphere;
|
|
|
With
Caswell No. 744A;
|
|
|
With
Caswell No. 744A; N,N,N-tributyl-1-butanaminium iodide;
In
N,N-dimethyl-formamide;
for 24h;
Inert atmosphere;
Heating;
|
|
|
With
Caswell No. 744A; sodium iodide;
In
N,N-dimethyl-formamide;
at 90 ℃;
for 12h;
Inert atmosphere;
|
|
|
With
Caswell No. 744A;
In
N,N-dimethyl-formamide;
at 90 ℃;
for 4h;
Inert atmosphere;
|
|
|
With
Caswell No. 744A;
In
acetonitrile;
for 48h;
Reflux;
Inert atmosphere;
|
|
|
With
Caswell No. 744A;
Schlenk technique;
Inert atmosphere;
|
|
|
With
Caswell No. 744A; tetrabutylammonium bromide;
In
acetonitrile;
for 24h;
Reflux;
|
|
|
With
Caswell No. 744A; tetrabutylammonium bromide;
In
acetonitrile;
for 36h;
Reflux;
|
-
-
52090-18-3
3-bromopropyltriethoxysilane
-
-
83315-69-9
3-azidopropyltriethoxysilane
| Conditions | Yield |
|---|---|
|
In
ethanol;
|
83315-69-9 Upstream products
-
5089-70-3
(3-chloropropyl)triethoxysilane
-
52090-18-3
3-bromopropyltriethoxysilane
-
57483-09-7
(3-iodopropyl)triethoxysilane
83315-69-9 Downstream products
-
1616428-68-2
C41 H44 N6 O4 S3 Si