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M8800

Sigma-Aldrich

Methanesulfonyl chloride

98%

Synonym(s):

Mesyl chloride

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About This Item

Linear Formula:
CH3SO2Cl
CAS Number:
124-63-0
Molecular Weight:
114.55
Beilstein:
506297
EC Number:
204-706-1
MDL number:
MFCD00007454
UNSPSC Code:
12352101
PubChem Substance ID:
329818071

Assay

98%

form

liquid

refractive index

n20/D 1.452 (lit.)

bp

60 °C/21 mmHg (lit.)

density

1.48 g/mL at 25 °C (lit.)

SMILES string

CS(Cl)(=O)=O

InChI

1S/CH3ClO2S/c1-5(2,3)4/h1H3

InChI key

QARBMVPHQWIHKH-UHFFFAOYSA-N

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Pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

Signal Word

Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B - Skin Sens. 1 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

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

WGK

WGK 2

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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E A Connor et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 3(11), 2164-2171 (1983-11-01)
Excitatory postsynaptic currents (EPSCs), miniature excitatory postsynaptic currents (MEPSCs), and acetylcholine-induced current fluctuations (noise) have been studied in voltage-clamped bullfrog parasympathetic ganglion cells of the atrial septum. EPSCs were also recorded from voltage-clamped sympathetic B cells and, in general, it
R Kullberg et al.
The Journal of physiology, 374, 413-427 (1986-05-01)
The development of miniature end-plate currents (m.e.p.c.s) was studied in the superior oblique and interhyoideus muscles of Xenopus laevis. An analysis of m.e.p.c. decays shows that each muscle possesses its own characteristic programme of end-plate current development. In the superior
Zdzisław Brzozowski et al.
Journal of medicinal chemistry, 45(2), 430-437 (2002-01-11)
A new series of 8-chloro-5,5-dioxoimidazo[1,2-b][1,4,2]benzodithiazine derivatives 8-25 with heteroaryloxycarbonyl or heteroarylcarbamoyl substituents at position 7 have been synthesized as potential antitumor agents. In this procedure a novel type of mixed anhydride 7 was prepared from 8-chloro-5,5-dioxoimidazo[1,2-b][1,4,2]benzodithiazine-7-carboxylic acid 6 and methanesulfonyl
Yasuhiro Torisawa et al.
Bioorganic & medicinal chemistry letters, 17(2), 453-455 (2006-10-27)
New and effective method for the Beckmann rearrangement of indanone oxime mesylate is described, in which a selective and controlled production of the isomeric isocarbostyrils is achieved.
Yasuhiro Torisawa et al.
Bioorganic & medicinal chemistry letters, 17(2), 448-452 (2006-10-28)
Continuing search for beneficial additive toward the Beckmann rearrangement (BR) of indanone oxime has revealed that common Lewis acid catalyst in methanesulfonyl chloride (MsCl) showed increasing efficiency in this ionic rearrangement. The new protocol with MsCl is superior to the
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