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Benzene, 1,1'-thiobis[2,3,5,6-tetrafluoro-4-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34883-24-4

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34883-24-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34883-24-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,8,8 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 34883-24:
(7*3)+(6*4)+(5*8)+(4*8)+(3*3)+(2*2)+(1*4)=134
134 % 10 = 4
So 34883-24-4 is a valid CAS Registry Number.

34883-24-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(4-nitro-2,3,5,6-tetrafluorophenyl) sulfide

1.2 Other means of identification

Product number -
Other names 4,4'-dinitro-octafluorodiphenyl sulfide

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:34883-24-4 SDS

34883-24-4Relevant academic research and scientific papers

Rhodium-catalyzed synthesis of diaryl sulfides using aryl fluorides and sulfur/organopolysulfides

Arisawa, Mieko,Ichikawa, Takuya,Yamaguchi, Masahiko

supporting information, p. 5318 - 5321 (2013/01/15)

Substituted pentafluorobenzenes react with sulfur to give bis(4-substituted 2,3,5,6-tetrafluorophenyl) sulfides in the presence of RhH(PPh 3)4, 1,2-bis(diphenylphosphino)benzene (dppBz), and tributylsilane. The reaction proceeds efficiently between room temperature and 80 °C. A comparative study of the reactivities of an organic trisulfide and a tetrasulfide showed notable substrate specificity. Di-tert-butyl tetrasulfide reacted with reactive aryl monofluorides and substituted pentafluorobenzenes. Di-tert-butyl trisulfide reacted with aryl monofluorides. The reactivity was explained on the basis of the difference in S-S bond energy.

An investigation into the haematological toxicity of structural analogues of dapsone in-vivo and in-vitro

Coleman,Tingle,Hussain,Storr,Park

, p. 779 - 784 (2007/10/02)

With microsomes prepared from a single human liver, 4,4'-diaminodiphenyl sulphone (DDS). 4-acetyl-4-aminodiphenyl sulphone (MADDS), 4-acetyl-4-aminodiphenyl thioether (MADDT) and 4,4'-diacetyldiphenyl thioether (DADDT) caused significantly greater methaem

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