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Heptane-3-sulfonylchloride, also known as 3-heptanesulfonyl chloride or 1-chloro-3-heptanesulfonic acid, is an organic compound with the chemical formula C7H15ClO2S. It is a colorless to pale yellow liquid with a pungent odor and is soluble in organic solvents. heptane-3-sulfonylchloride is a derivative of heptane, where a sulfonyl chloride group replaces one of the hydrogen atoms on the third carbon. Heptane-3-sulfonylchloride is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also employed in the preparation of sulfonamide drugs and as a reagent in organic synthesis. Due to its reactivity, it is essential to handle heptane-3-sulfonylchloride with care, using appropriate safety measures and protective equipment.

1069-34-7

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1069-34-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1069-34-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,6 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1069-34:
(6*1)+(5*0)+(4*6)+(3*9)+(2*3)+(1*4)=67
67 % 10 = 7
So 1069-34-7 is a valid CAS Registry Number.

1069-34-7Upstream product

1069-34-7Downstream Products

1069-34-7Relevant articles and documents

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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