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73318-12-4

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73318-12-4 Usage

Type of compound

Nitrobenzene derivative

Structural feature

Benzylsulfinyl methyl group attached to the fourth position of the nitrobenzene ring

Usage

Precursor in the synthesis of pharmaceuticals and agrochemicals

Importance

Presence of the nitro group makes it an important intermediate in the production of various organic compounds and materials

Value

Chemical structure and properties make it a valuable building block for the development of new drugs and agricultural products

Check Digit Verification of cas no

The CAS Registry Mumber 73318-12-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,3,1 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 73318-12:
(7*7)+(6*3)+(5*3)+(4*1)+(3*8)+(2*1)+(1*2)=114
114 % 10 = 4
So 73318-12-4 is a valid CAS Registry Number.

73318-12-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(benzylsulfinylmethyl)-4-nitrobenzene

1.2 Other means of identification

Product number -
Other names benzyl-(4-nitro-benzyl)-sulfoxide

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:73318-12-4 SDS

73318-12-4Relevant articles and documents

Synthesis and characterization of Manganese(III) tetraphenylporphyrinato chloride immobilized on multi-wall carbon nanotubes, and its application as an efficient and reusable catalyst in the biomimetic oxidation of sulfides: A comprehensive experimental and computational study

Khajehzadeh, Mostafa,Moghadam, Majid,Noorbakhsh, Pardis

, (2020/08/07)

In the present study, manganese(III) tetraphenylporphyrinato choloride, was immobilized on multiwall carbon nanotubes by covalent bonding. The structures of [Mn(TPP)Cl]&at;AP-MWC catalyst was confirmed by FT-IR, UV–vis spectroscopic techniques and scanning electron microscopy (SEM). Then, the ability of this novel heterogeneous catalyst was investigated in the oxidation of linear and cyclic sulfides under magnetic stirring conditions. Also, the DFT computational method (B3PW91 method with LanL2DZ basis set) was used for further analysis of this catalyst. Based on this method, the molecular geometries and frequencies of vibrations, chemical shifts, absorbed wavelengths, hyper-conjugative interactions, electron transitions between electron surfaces, positive and negative charges, HOMO and LUMO gap, wavelength (λ), chemical potential (μ), ionization energy (IE), global hardness (η), global softness (S), electrophilicity index (ω) and electronegativity (α) of the most intensity electronic transition for carbon nanotubes and [Mn(TPP)Cl]&at;AP-MWCNT catalyst were calculated. The activity and efficiency of this catalyst were then investigated in the biomimetic oxidation of sulfides. The [Mn(TPP)Cl]&at;AP-MWC heterogeneous catalyst showed the advantages such as high efficiency, good to excellent yield, short reaction times, easy separation and high reusability of the catalyst.

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