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4-iodo-phenyl thiocyanate is an organic compound with the chemical formula C7H4INS. It is a derivative of phenyl thiocyanate, where one of the hydrogen atoms on the phenyl ring is replaced by an iodine atom. This halogenated compound is characterized by its yellowish color and is often used as a reagent in organic synthesis. It is soluble in organic solvents and has a melting point of approximately 70-72°C. Due to the presence of the iodine atom, 4-iodo-phenyl thiocyanate can participate in various chemical reactions, such as nucleophilic substitutions and coupling reactions, making it a valuable intermediate in the synthesis of more complex molecules.

3321-93-5

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3321-93-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3321-93-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,2 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3321-93:
(6*3)+(5*3)+(4*2)+(3*1)+(2*9)+(1*3)=65
65 % 10 = 5
So 3321-93-5 is a valid CAS Registry Number.

3321-93-5SDS

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 4-iodo-phenyl thiocyanate

1.2 Other means of identification

Product number -
Other names 4-Jod-phenylrhodanid

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:3321-93-5 SDS

3321-93-5Relevant academic research and scientific papers

Highly efficient Sandmeyer reaction on immobilized CuI/CuII-based catalysts

Tarkhanova, Irina G.,Gantman, Michail G.,Sigeev, Alexander S.,Maslakov, Konstantin I.,Zelikman, Vladimir M.,Beletskaya, Irina P.

, p. 261 - 263 (2018/06/01)

Highly effective embodiment of Sandmeyer reaction has been revealed for Cu-based catalysts incorporating ionic liquid on Silochrom support. The most active catalyst (TOF = = 4000–8000 h–1) contains comparable amounts of cuprous and cupric chloride anions. The reported method allows one to carry out the reaction for anilines in the one-pot mode.

Improved procedure to aryl thiocyanates: A new synthetic application of dry arenediazonium o-benzenedisulfonimides

Barbero,Degani,Diulgheroff,Dughera,Fochi

, p. 585 - 590 (2007/10/03)

Aryl thiocyanates 3 (22 examples) were easily prepared by reaction of dry arenediazonium o-benzenedisulfonimides 1 and sodium thiocyanate (2) in anhydrous acetonitrile at room temperature (20-25 °C) in the presence of copper powder (Procedure A) and at 50 °C or room temperature without the metal catalyst (Procedure B). The yields were from very good to excellent in Procedure A (average yield = 83%), and from modest to excellent in Procedure B (average yield = 63%). In comparison with the thiocyanod-ediazoniation carried out under traditional Sandmeyer-type conditions, the yields of 3 were higher and the isothiocyanate isomers were formed only in traces. Moreover, the results obtained in the absence of copper confirm the role of the anion of salts 1 as an electron transfer agent.

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