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N-[(2-nitrophenyl)sulfanyl]aniline, also known as 2-nitrophenylsulfanylaniline, is an organic compound with the chemical formula C12H10N2O2S. It is a yellow crystalline solid that is soluble in organic solvents such as ethanol and acetone. N-[(2-nitrophenyl)sulfanyl]aniline is characterized by the presence of an aniline group (C6H5NH2) and a 2-nitrophenyl group (C6H4NO2) connected through a sulfur atom, forming a sulfanyl (-S-) linkage. It is primarily used as an intermediate in the synthesis of various dyes, pigments, and pharmaceuticals. Due to its chemical structure, it exhibits properties such as reactivity towards electrophilic aromatic substitution and potential toxicity due to the presence of the nitro group.

4837-33-6

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4837-33-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4837-33-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,3 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4837-33:
(6*4)+(5*8)+(4*3)+(3*7)+(2*3)+(1*3)=106
106 % 10 = 6
So 4837-33-6 is a valid CAS Registry Number.

4837-33-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-nitrophenyl)sulfanylaniline

1.2 Other means of identification

Product number -
Other names N-Phenyl-o-nitro-benzolsulfenamid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4837-33-6 SDS

4837-33-6Relevant academic research and scientific papers

Organocatalytic Allylic Amination of Morita-Baylis-Hillman Carbonates

Formánek, Bed?ich,?imek, Michal,Kamlar, Martin,Císa?ová, Ivana,Vesely, Jan

, p. 907 - 920 (2019/02/10)

An organocatalytic asymmetric allylic amination of Morita-Baylis-Hillman carbonates with aromatic amines in the presence of β-isocupreidine is described. Chiral allylic amines were obtained in almost quantitative yields (90-96%) with moderate enantioselectivity. Recrystallization afforded products in good yields (45-73%) and high optical purity (82-99% ee). This method provides a facile and efficient route to obtain optically active β-lactams, including the building block of the cholesterol-lowering drug Ezetimibe.

Silver ion mediated in situ synthesis of mixed diaryl sulfides from diaryl disulfides

Gogoi, Prasanta,Gogoi, Sandhya R.,Kalita, Mukul,Barman, Pranjit

, p. 873 - 877 (2013/05/21)

The AgNO3-mediated in situ scission of aromatic disulfides in the presence of electron-rich aromatic compounds results in the efficient synthesis of diaryl sulfides. Key features of this new methodology are high yields of aromatic and heteroaromatic sulfides, mild reaction conditions, simplicity, simple workup, and avoiding foul-smelling reactants like thiols. Georg Thieme Verlag Stuttgart · New York.

The orthopalladation of aniline via its 2-nitrophenylsulfenyl derivative

Guarnieri, A.,Parkins, A. W.

, p. 399 - 404 (2007/10/02)

2-Nitrophenylsulfenylanilide can be orthopalladated to give μ,μ-dichlorodipalladium-bis(2-nitrophenylsulfenylanilide), which on carbometoxylation gives 2-nitrophenylsulfenylanthranylate.

Ortho Effects in Organic Molecules on Electron Impact: 21 - Oxygen Transfers from the Ortho Nitro Group to Sulphur in N-Aryl-2-nitrobenzenesulphenamides and Phenyl-2-nitrophenyl Disulphide

Ramana, D. V.,Sundaram, N.,George, M.

, p. 926 - 930 (2007/10/02)

Fragment ions arising as a result of oxygen transfer from the nito group to sulphur have been noticed in N-aryl-2-nitrobenzenesulphenamides and phenyl-2-nitrophenyl disulphide.In the case of the former a double oxygen transfer to the sulphur has been noti

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