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(2-Iodophenyl)methanesulphonyl chloride, also known as IMS, is a chemical compound with the molecular formula C7H6ClIO2S. It is a versatile and important reagent in organic chemistry due to its ability to introduce the methanesulfonyl group onto various organic molecules. However, it should be handled with caution as it is a corrosive and toxic compound.

25068-94-4

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25068-94-4 Usage

Uses

Used in Organic Synthesis:
IMS is used as a reagent for the preparation of various sulfonamides and sulfones. It reacts with amines to form sulfonamides, and with lithium aluminum hydride to form a methanesulfonyl group.
Used in Pharmaceutical Industry:
IMS is used in the pharmaceutical industry for the production of drugs. Its ability to introduce the methanesulfonyl group onto various organic molecules makes it a valuable tool in drug synthesis.
Used in Research Laboratories:
IMS is utilized in research laboratories for the synthesis of various organic compounds. Its versatility and reactivity make it an important reagent in the development of new organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 25068-94-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,0,6 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 25068-94:
(7*2)+(6*5)+(5*0)+(4*6)+(3*8)+(2*9)+(1*4)=114
114 % 10 = 4
So 25068-94-4 is a valid CAS Registry Number.

25068-94-4Upstream product

25068-94-4Relevant academic research and scientific papers

HERBICIDAL COMPOUNDS

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Page/Page column 49, (2009/06/27)

The present invention relates to compounds of formula (I), wherein R1, R2, R3, R4 and R5 are as defined in claim 1; or a salt or N-oxide thereof. Furthermore, the present invention relates to processe

Brominative indolization of an unsaturated bridgehead sultam with extrusion of sulfur dioxide

Preston, Adam J,Paquette, Leo A.

, p. 41 - 44 (2007/10/03)

The dissolution of an unsaturated bridgehead sultam in liquid bromine at room temperature results in the formation of a pentabromo indole derivative in an unusual desulfonylative process.

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