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(p-Chlorophenyl)methanesulfonyl fluoride, also known as (p-chlorophenyl)methylsulfonyl fluoride or PMSF, is a potent irreversible serine protease inhibitor commonly used in biochemistry and molecular biology. It works by forming a covalent bond with the active site serine residue of the enzyme, thereby inhibiting its activity. PMSF is particularly useful for preventing proteolysis in cell lysates and other biological samples, as it can effectively block the action of various proteases, including trypsin, chymotrypsin, and elastase. It is often used in conjunction with other protease inhibitors to ensure complete inhibition of proteolytic activity. PMSF is a colorless, crystalline solid that is soluble in organic solvents and water, and it is typically used at concentrations ranging from 0.1 to 1 mM. Due to its reactivity, PMSF must be handled with care and used in a fume hood to prevent inhalation or skin contact.

1513-29-7

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1513-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1513-29-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,1 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1513-29:
(6*1)+(5*5)+(4*1)+(3*3)+(2*2)+(1*9)=57
57 % 10 = 7
So 1513-29-7 is a valid CAS Registry Number.

1513-29-7Relevant academic research and scientific papers

Sulfonyl Fluoride Synthesis through Electrochemical Oxidative Coupling of Thiols and Potassium Fluoride

Laudadio, Gabriele,Bartolomeu, Aloisio De A.,Verwijlen, Lucas M. H. M.,Cao, Yiran,De Oliveira, Kleber T.,No?l, Timothy

, p. 11832 - 11836 (2019)

Sulfonyl fluorides are valuable synthetic motifs for a variety of applications, among which sulfur(VI) fluoride exchange-based "click chemistry" is currently the most prominent. Consequently, the development of novel and efficient synthetic methods to access these functional groups is of great interest. Herein, we report a mild and environmentally benign electrochemical approach to prepare sulfonyl fluorides using thiols or disulfides, as widely available starting materials, in combination with KF, as an inexpensive, abundant and safe fluoride source. No additional oxidants nor additional catalysts are required and, due to mild reaction conditions, the reaction displays a broad substrate scope, including a variety of alkyl, benzyl, aryl and heteroaryl thiols or disulfides.

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