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178950

Sigma-Aldrich

Methansulfonylfluorid

98%

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About This Item

Lineare Formel:
CH3SO2F
CAS-Nummer:
558-25-8
Molekulargewicht:
98.10
EG-Nummer:
209-192-2
MDL-Nummer:
MFCD00007423
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24850783

Assay

98%

Eignung der Reaktion

reaction type: click chemistry

bp

123-124 °C (lit.)

Dichte

1.427 g/mL at 25 °C (lit.)

SMILES String

CS(F)(=O)=O

InChI

1S/CH3FO2S/c1-5(2,3)4/h1H3

InChIKey

KNWQLFOXPQZGPX-UHFFFAOYSA-N

Allgemeine Beschreibung

Methanesulfonyl fluoride is an anticholinesterase (antiChEs), used to treat Alzheimer′s disease. It is a thrombin inhibitor.

Zubehör

Produkt-Nr.
Beschreibung
Preisangaben

Piktogramme

Skull and crossbonesCorrosion
GHS06,GHS05

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 2 Oral - Skin Corr. 1B

Lagerklassenschlüssel

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Analysenzertifikate (COA)

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D H Malin et al.
Neurobiology of aging, 12(2), 181-183 (1991-03-01)
In previous studies, 18-month-old rats have shown no significant retention 24 hours after the single acquisition trial in a one-trial discriminative reward learning task. In the present study, ten 18-month-old rats pretreated with 0.5 mg/kg MSF IP showed significantly better
Navid Jamali et al.
Reproductive sciences (Thousand Oaks, Calif.), 28(3), 683-692 (2020-11-04)
Endometriosis, as the leading cause of infertility, is attributed to oxidative stress, inflammation, and autophagy dysregulation. This study was conducted to evaluate the effect of quercetin and metformin, alone or in combination, on the ectopic and eutopic endometrial tissues in
P Masson et al.
Biochimica et biophysica acta, 869(3), 304-313 (1986-02-14)
In order to determine whether a structural modification at the active center of cholinesterase may alter the conformational stability of the enzyme we compared the urea-induced unfolding of the tetrameric form of non-inhibited and irreversibly inhibited human plasma cholinesterase (acylcholine
M Zorko et al.
Biochemical pharmacology, 35(14), 2287-2296 (1986-07-15)
The binding of D-tubocurarine (TC) to acetylcholinesterase (AChE) was studied using different methods of enzyme kinetics. The main results are as follows. TC reversibly inhibits the hydrolysis of different substrates of AChE with three different inhibition constants (Ki1 = 7.0
R Panenic et al.
Journal of applied physiology (Bethesda, Md. : 1985), 87(4), 1455-1462 (1999-10-12)
The purpose of this study was to investigate the functional impact of acute irreversible inhibition of acetylcholinesterase (AChE) on the fatigability of medial gastrocnemius and plantaris muscles of Sprague-Dawley rats. After treatment with methanesulfonyl fluoride (a lipid-soluble anticholinesterase), which reduced
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