Log In Sign up
The largest database of trusted experimental protocols

4 vinylaniline

Manufactured by Merck Group
Visit Supplier

4-vinylaniline is a chemical compound used as a laboratory reagent. It serves as a precursor for various organic synthesis reactions. The compound has a benzene ring structure with a vinyl group and an amino group attached. 4-vinylaniline is a colorless to pale yellow liquid with a characteristic amine-like odor. It is soluble in organic solvents and finds application in the production of polymers and other chemical intermediates.

Automatically generated - may contain errors

Lab products found in correlation

Tetrabutylammonium bromide, by Merck Group (1 mentions) Tetrabutylammonium iodide, by Merck Group (1 mentions) 2 aminoethyl methacrylate hydrochloride, by Merck Group (1 mentions) Zinc trifluoromethanesulfonate, by Merck Group (1 mentions) Tetrabutylammonium chloride, by Merck Group (1 mentions) Ethylene glycol dimethacrylate egdma, by Merck Group (1 mentions) 2 2 azobis 2 methylpropionitrile aibn, by Merck Group (1 mentions) N n diisopropylethylamine dipea, by Merck Group (1 mentions) N n dimethyl acrylamide dmaam, by Merck Group (1 mentions) Lead iodide, by Merck Group (1 mentions) Tetradecane, by Merck Group (1 mentions) Aqueous hydriodic acid, by Merck Group (1 mentions) Benzoyl peroxide, by Merck Group (1 mentions) Potassium iodide, by Merck Group (1 mentions) Deuterium oxide d2o, by Merck Group (1 mentions) Lead bromide, by Merck Group (1 mentions)

2 protocols using 4 vinylaniline

1

Synthesis of Functional Polymeric Materials

Check if the same lab product or an alternative is used in the 5 most similar protocols
Unless otherwise indicated, all solvents
were purchased from commercial sources and were used without further
purification. 3,4-Diethoxycyclobut-3-ene-1,2-dione (95%, ABCR), zinc
trifluoromethanesulfonate (98%, Sigma-Aldrich), 4-vinylaniline (97%,
Sigma-Aldrich), 2-aminoethyl methacrylate hydrochloride (90%, Sigma-Aldrich), N,N-diisopropylethylamine (DIPEA, >99%,
Sigma-Aldrich), N,N-dimethylacrylamide
(DMAAm, 99%, Sigma-Aldrich), ethylene glycol dimethacrylate (EGDMA,
98%, Sigma-Aldrich), 2,2′-azobis(2-methylpropionitrile) (AIBN,
98%, Sigma-Aldrich), tetrabutylammonium fluoride hydrate ([Bu4N]+[F]−, 98%, ABCR), tetrabutylammonium
chloride ([Bu4N]+[Cl]−, >97%,
Sigma-Aldrich), tetrabutylammonium bromide ([Bu4N]+[Br]−, >98%, Sigma-Aldrich), tetrabutylammonium
iodide ([Bu4N]+[I]−, 98%,
Sigma-Aldrich), and tetrabutylammonium acetate ([Bu4N]+[AcO]−, 95%, ABCR) were used as received.
AIBN was recrystallized from methanol prior to use and stored below
5 °C. To remove the residual inhibitor, the main monomer DMAAm
was destabilized via a short column of basic alumina prior use.
Mommer S, & Wezenberg S.J. (2022). Anion-Induced Reversible Actuation of Squaramide-Crosslinked Polymer Gels. ACS Applied Materials & Interfaces, 14(38), 43711-43718.
+ Open protocol
+ Expand
2

Synthesis of Organolead Halide Perovskites

Check if the same lab product or an alternative is used in the 5 most similar protocols
MilliQ water was obtained using an IQ 7000 purifying system. Ethanol absolute (analytical grade), tetrahydrofuran anhydrous 99.99 % (THF), diethyl ether (puriss. p.a. ACS reagent dried 0.05 % GC 0.0075 % water) and hexane (HPLC grade) were purchased from Scharlau. 4-Vinylaniline (97%), tetradecane (≥ 99 %), aqueous hydriodic acid (HI, 55 wt%), lead iodide (99.999 % trace metals basis, PbI2), benzoyl peroxide (75%), lead bromide (99.999 % trace metals basis, PbBr2), potassium iodide (99.5%, KI) and deuterium oxide (D2O) were purchased from Sigma Aldrich. All solvents and reagents were used without further purification.
Peng Y ., Albero J , & Garcia H . (2020). Synthesis, post-synthetic modification and stability of a 2D styryl ammonium lead iodide hybrid material. Dalton transactions (Cambridge, England : 2003), 49(2).
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!