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Benzenesulfenamide, 4-nitro-N-phenyl-, also known as 4-nitro-N-phenylbenzenesulfenamide, is an organic compound with the chemical formula C12H10N2O2S. It is a derivative of benzenesulfenamide, featuring a nitro group (-NO2) at the para position of the phenyl ring attached to the sulfenamide group. This yellow crystalline solid is primarily used as a vulcanization accelerator in the rubber industry, enhancing the strength and elasticity of rubber products. It is also known for its applications in the production of adhesives and coatings. Due to its reactivity, it is important to handle this chemical with care, following proper safety protocols to minimize potential health and environmental risks.

5147-60-4

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5147-60-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5147-60-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,4 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5147-60:
(6*5)+(5*1)+(4*4)+(3*7)+(2*6)+(1*0)=84
84 % 10 = 4
So 5147-60-4 is a valid CAS Registry Number.

5147-60-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-nitrobenzensulfenic acid anilide

1.2 Other means of identification

Product number -
Other names 4-Nitro-benzolsulfensaeure-anilid

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:5147-60-4 SDS

5147-60-4Relevant academic research and scientific papers

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 (1989)

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

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.

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