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S-propyl benzenethiosulfonate, also known as S-propyl tosylamide or PTA, is an organic compound with the chemical formula C10H13NOS2. It is a colorless, crystalline solid that is soluble in organic solvents. PTA is primarily used as a reagent in organic synthesis, particularly in the preparation of various heterocyclic compounds and as a protecting group in peptide synthesis. It is also employed as a selective inhibitor of certain enzymes, such as acetylcholinesterase, and has been studied for its potential applications in pharmaceutical research. Due to its reactivity and potential toxicity, PTA should be handled with care and used in accordance with appropriate safety guidelines.

5184-58-7

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5184-58-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5184-58-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,8 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5184-58:
(6*5)+(5*1)+(4*8)+(3*4)+(2*5)+(1*8)=97
97 % 10 = 7
So 5184-58-7 is a valid CAS Registry Number.

5184-58-7Downstream Products

5184-58-7Relevant academic research and scientific papers

Copper-Catalyzed Oxidative Trifunctionalization of Olefins: An Access to Functionalized β-Keto Thiosulfones

Huang, Shuai,Thirupathi, Nuligonda,Tung, Chen-Ho,Xu, Zhenghu

, p. 9449 - 9455 (2018/08/01)

Aerobic oxidative trifunctionalization of olefins for the synthesis of functionalized β-keto thiosulfones has been described. The transformation proceeds through molecular oxygen activation under copper catalysis and forms the two new C-S bonds in a single operation using mild conditions. A novel Cu-catalyzed sulfonyl radical addition/oxidation/funtionalization relay mechanism was proposed for the discovered reaction.

Selective Oxidation of Unsymmetrical Thiosulfinic S-Esters to the Corresponding Thiosulfonic S-Esters with NaIO4

Takata, Toshikazu,Kim, Yong Hae,Oae, Shigeru

, p. 1443 - 1447 (2007/10/02)

Unsymmetrical thiosulfinic S-esters were oxidized with sodium metaperiodate in aqueous media to the corresponding unsymmetrical thiosulfonic S-esters nearly quantitatively.The oxidation was accelerated by addition of a catalytic amount of inorganic and organic acids or halogen.Sulfinic esters were produced competitively along with the thiosulfonic S-esters in the oxidation of thiosulfinic S-esters in aqueous alcohol.However, unsymmetrical disulfides were not oxidized selectively to the corresponding unsymmetrical thiosufonic S-esters but a mixture of the both symmetrical and unsymmetrical thiosulfonic S-esters was obtained.

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