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4-iodophenyl carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

329709-91-3

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329709-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 329709-91-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,9,7,0 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 329709-91:
(8*3)+(7*2)+(6*9)+(5*7)+(4*0)+(3*9)+(2*9)+(1*1)=173
173 % 10 = 3
So 329709-91-3 is a valid CAS Registry Number.

329709-91-3Downstream Products

329709-91-3Relevant academic research and scientific papers

Superparamagnetic Fe3O4 Nanoparticles in a Deep Eutectic Solvent: An Efficient and Recyclable Catalytic System for the Synthesis of Primary Carbamates and Monosubstituted Ureas

Inaloo, Iman Dindarloo,Majnooni, Sahar,Esmaeilpour, Mohsen

, p. 3481 - 3488 (2018/07/29)

Superparamagnetic Fe3O4 nanoparticles were used to synthesize various primary carbamates as well as monosubstituted and N,N-disubstituted ureas. This efficient phosgene-free process used urea as an eco-friendly carbonyl source in the presence of a biocompatible deep eutectic solvent (DES) to provide an inexpensive and attractive route that afforded the products in moderate to excellent yields. The employed DES serves both a catalytic role and as the green reaction medium. The magnetic nanocatalyst and DES can been reused several times without a significant loss of activity.

4-Dodecylbenzenesulfonic acid (DBSA) promoted solvent-free diversity-oriented synthesis of primary carbamates, S-thiocarbamates and ureas

Sardarian, Ali Reza,Inaloo, Iman Dindarloo

, p. 76626 - 76641 (2015/09/22)

A simple and highly efficient solvent-free method for the conversion of alcohols, phenols, thiols and amines to primary carbamates, S-thiocarbamates and ureas in the presence of 4-dodecylbenzenesulfonic acid (DBSA) as a cheap and green Bronsted acid reagent has been described. All products were obtained in good to excellent yields and characterized using FT-IR, 1H- and 13C-NMR, MS and CHNS techniques.

Hybrid calix[4]arenes via ionic hydrogenation and transition-metal-mediated processes

Bew, Sean P.,Brimage, Rebecca A.,Hiatt-Gipson, Glyn,Sharma, Sunil V.,Thurston, Sean

supporting information; experimental part, p. 2483 - 2486 (2009/10/18)

We report the first application of ionic hydrogenation for the synthesis of upper-rim urea- or carbamate-derived hybrid calix[4]arenes. Subsequent metal-mediated transformations using 4-iodophenylurea calixarenes afforded structurally unique 1,3-di(biaryl)-, 1,3-di(biarylalkyne)-, or 1,3-(biaryl)(biarylalkyne)-derived hybrid calixarenes.

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