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2-Chlorosulfonyl heptane, also known as 1-heptanesulfonyl chloride, is an organic compound with the chemical formula C7H15ClO2S. It is a colorless to pale yellow liquid that is soluble in organic solvents. 2-chlorosulfonyl heptane is a derivative of heptane, with a sulfonyl chloride group (-SO2Cl) attached to the second carbon atom. 2-Chlorosulfonyl heptane is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also employed as a reagent in the preparation of sulfonamides and other sulfur-containing compounds. Due to its reactivity, it is essential to handle 2-chlorosulfonyl heptane with care, as it can be harmful if inhaled, ingested, or absorbed through the skin.

922-76-9

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922-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 922-76-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 922-76:
(5*9)+(4*2)+(3*2)+(2*7)+(1*6)=79
79 % 10 = 9
So 922-76-9 is a valid CAS Registry Number.

922-76-9Upstream product

922-76-9Downstream Products

922-76-9Relevant academic research and scientific papers

Cobalt(II)-Porphyrin Catalyzed Selective Functionalization of Alkanes with sulfurylchloride: A Remarkable Substituent Effect

Khanna, Vibha,Tamilselvan, Pitchiah,Kalra, Swinder Jeet Singh,Iqbal, Javed

, p. 5935 - 5938 (1994)

Cobalt(II)-porphyrin complex 1 and 2 catalyses the chlorination and sulfochlorination respectively of n-alkanes and cycloalkanes with sulfuryl chloride in benzene.The p-substituent of the benzene ring in the porphyrin complex 1 and 2 shows a remarkable chemoselectivity in these reactions.

THE PHOTOCHEMICAL CHLOROSULFONATION OF HEPTANE BY SULFURYL CHLORIDE. THE ROLE OF SOLVENT AND CATALYST. A REINVESTIGATION.

Tazerouti, A.,Rahal, S.,Soumillion, J. Ph.

, p. 101 - 119 (2007/10/02)

Sulfuryl chloride has been tested as a chlorosulfonation reagent of n-heptane under various conditions.Pyridine was confirmed as the best catalyst for the reaction and the sulfochlorination yield was found to be enhanced by the use of benzene as solvent.The distribution of all the isomeric chlorinated and sulfochlorinated products has been measured.This information is used in order to understand the mechanism of this rather complex reaction.The catalyzed photoinitiation leads to the in situ formation of a low concentration of molecular chlorine.The observed selectivity is the result of a delicate balance between the photoinitiation leading the chlorine atoms and the rather short chain propagations leading to the formation of the chlorosulfonyl radical.

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