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Cyclohexyl benzenesulphonate, also known as cyclohexyl benzenesulfonate, is an organic compound with the chemical formula C12H17SO3. It is a white crystalline solid that is soluble in water and various organic solvents. Cyclohexyl benzenesulphonate is primarily used as a surfactant in detergents, emulsifiers, and wetting agents due to its ability to lower surface tension and improve the solubility of other substances. Cyclohexyl benzenesulphonate is also employed in the manufacturing of personal care products, such as shampoos and soaps, as well as in industrial applications like textile processing and metal cleaning. Its chemical structure consists of a cyclohexane ring attached to a benzene ring, with a sulfonate group (-SO3H) connected to the benzene ring, providing it with its surfactant properties.

782-84-3

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782-84-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 782-84-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,8 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 782-84:
(5*7)+(4*8)+(3*2)+(2*8)+(1*4)=93
93 % 10 = 3
So 782-84-3 is a valid CAS Registry Number.

782-84-3Relevant academic research and scientific papers

CsF-Celite as an efficient heterogeneous catalyst for sulfonylation and desulfonylation of heteroatoms

Tamaddon, Fatemeh,Nasiri, Alireza,Farokhi, Somayeh

experimental part, p. 1477 - 1482 (2012/06/18)

CsF-Celite is found to be as an efficient reusable catalyst for sulfonylation and desulfonylation of heteroatoms. Sulfonamides and N-acylsulfonamides deprotect efficiently in the presence of CsF-Celite under solvent free conditions to give the free amines or amides in good to excellent yields.

An efficient one-pot conversion of THP and TMS ethers to sulfonate esters using FeCl3-montmorillonite K-10 clay

Movassagh, Barahman,Shokri, Salman

, p. 763 - 765 (2007/10/03)

Various tetrahydropyranyl and trimethylsilyl ethers are efficiently transformed into the corresponding sulfonate esters with sulfonyl chlorides in the presence of FeCl3-Montmorillonite K-10 clay.

Montmorillonite clay catalyzed tosylation of alcohols and selective monotosylation of diols with p-toluenesulfonic acid: An enviro-economic route

Choudary, Boyapati M.,Chowdari, Naidu S.,Kantam, Mannepalli L.

, p. 7291 - 7298 (2007/10/03)

An enviro-economic route for tosylation of alcohols and selective monotosylation of diols in good yield directly using p-toluenesulfonic acid together with metal-exchanged montmorillonite instead of p-toluenesulfonyl chloride or p-toluenesulfonic anhydrid

2,2-Bis(ethylthio)ethanenitrile: preparation and use as a one or two carbon nucleophile

Bates, Gordon S.,Ramaswamy, S.

, p. 2006 - 2009 (2007/10/02)

2,2-Bis(ethylthio)ethanenitrile 1 was prepared in high yield from 2,2-bis(ethylthio)ethanal 2.Alkylation of the potassium salt of 1 with various alkylating agents and conjugate addition to cyclic α,β-unsaturated ketones provided high yields of the alkylation products of 1.The potential one and two carbon chain extension capability of this new reagent has been demonstrated.

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