4 nitroaniline

Manufactured by Johnson & Johnson

Sourced in Belgium

4-nitroaniline is a chemical compound used in laboratory settings. It is a crystalline solid that is soluble in organic solvents. This product is primarily utilized as a chemical intermediate for various applications.

Automatically generated - may contain errors

Lab products found in correlation

Cyclohexylamine, by Merck Group (2 mentions) Triethylamine, by Tedia (2 mentions) Dimethylformamide, by Carlo Erba (2 mentions) Sulfaguanidine, by Tokyo Chemical Industry (2 mentions) Morpholine, by Tokyo Chemical Industry (2 mentions) M toluidine, by Merck Group (2 mentions) 4 chloroaniline, by Merck Group (2 mentions) 4 bromoaniline, by Merck Group (2 mentions) 4 fluoroaniline, by Merck Group (2 mentions) N hexane, by Carlo Erba (2 mentions) Ethanol, by Carlo Erba (2 mentions) Acetone, by Carlo Erba (2 mentions) Chloroform, by Carlo Erba (2 mentions) Dimethyl sulfoxide (dmso), by Carlo Erba (2 mentions) 2 aminobenzothiazole, by Merck Group (1 mentions) Cyclopropylamine, by Merck Group (1 mentions)

2 protocols using 4 nitroaniline

Synthesis and Characterization of Benzothiazole Derivatives

Check if the same lab product or an alternative is used in the 5 most similar protocols

All reagents, catalysts,
and chemicals utilized in the study were of analytical quality and
supplied by commercial providers. The chemicals used in this study
were sourced from various suppliers. 2-Aminobenzothiazole (Sigma-Aldrich,
99%), sulfapyridine (NENTECH, U.K., 99%), sulfaguanidine (Tokyo Chemical
Industry, Japan, 98%), piperazine (Central Dreug House, India, 99%),
benzylamine (Loba Chemi, India, 99%), cyclohexylamine (Sigma-Aldrich,
99%), 3,4 dimethylaniline (GCC, U.K., 98%), 4-chloroaniline (Sigma-Aldrich,
98%), 4-bromoaniline (Sigma-Aldrich, 90%), 4-fluoroaniline (Sigma-Aldrich,
99%), 4-nitroaniline (Janssen, Belgium, 98%), diethylamine (GCC, U.K.,
98%), m-toluidine (Sigma-Aldrich, 99%), morpholine
(Tokyo Chemical Industry, Japan, 99%), dimethylformamide (DMF) (Carlo
Erba, France, 99.9%), acetone (Carlo Erba, France, 99%), triethylamine
(TEA) (TEDIA, 99%), ethanol (Carlo Erba, France, 98%), n-hexane (Carlo Erba, France, 95%), sodium bicarbonate (NaHCO₃) (GCC, U.K., 99.5%), sodium hydroxide (NaOH) (GCC, U.K.,
99.5%), chloroform (Carlo Erba, France, 99.9%), and dimethyl sulfoxide
(DMSO) (Carlo Erba, France, 99%) and monochloroacetyl chloride (α
Chemika, India) were used.

Salih O.M., Al-Sha’er M.A, & Basheer H.A. (2024). Novel 2-Aminobenzothiazole Derivatives: Docking, Synthesis, and Biological Evaluation as Anticancer Agents. ACS Omega, 9(12), 13928-13950.

+ Open protocol

+ Expand

Synthesis and Characterization of Sulfanilamide Derivatives

Check if the same lab product or an alternative is used in the 5 most similar protocols

All of the reagents and
chemicals were of analytical grade and purchased from commercial suppliers.
Sulfapyridine (NENTECH, U.K., 99%), sulfaguanidine (Tokyo Chemical
Industry, Japan, 98%), cyanuric chloride (Acros Organics, China, 99%),
aniline (GCC, U.K., 99.5%), benzylamine (LobaChemi, India, 99%), cyclopropylamine
(Sigma-Aldrich, 98%), cyclohexyl amine (Sigma-Aldrich, 99%), diethylamine
(GCC, U.K., 98%), m-toluidine (Sigma-Aldrich, 99%),
3,4-dimethylaniline (GCC, U.K., 98%), 4-chloroaniline (Sigma-Aldrich,
98%), 4-bromoaniline (Sigma-Aldrich, 90%), 4-fluoroaniline (Sigma-Aldrich,
99%), 4-nitroaniline (Janssen, Belgium, 98%), morpholine (Tokyo Chemical
Industry, Japan, 99%), acetone (Carlo Erba, France, 99%), ethanol
(Carlo Erba, France, 98%), dimethylformamide (DMF) (Carlo Erba, France,
99.9%), n-hexane (Carlo Erba, France, 95%), sodium
bicarbonate (NaHCO₃) (GCC, U.K., 99.5%), sodium hydroxide
(NaOH) (GCC, U.K., 99.5%), triethylamine (TEA) (TEDIA, 99%), chloroform
(Carlo Erba, France, 99.9%) and dimethyl sulfoxide (DMSO) (Carlo Erba,
France, 99%).

Alelaimat M.A., Al-Sha’er M.A, & Basheer H.A. (2023). Novel Sulfonamide–Triazine Hybrid Derivatives: Docking, Synthesis, and Biological Evaluation as Anticancer Agents. ACS Omega, 8(15), 14247-14263.

+ 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?

Revolutionizing how scientists
search and build protocols!