Skip to Content
Merck
CN

550256

Silver methanesulfonate

solid

Synonym(s):

Silver methylsulfonate, Methanesulfonic acid silver salt

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
AgSO3CH3
CAS Number:
Molecular Weight:
202.97
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12161600
EC Number:
219-199-2
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


Product Name

Silver methanesulfonate,

form

solid

Quality Level

reaction suitability

core: silver, reagent type: catalyst

mp

252-256 °C (lit.)

SMILES string

[Ag+].CS([O-])(=O)=O

InChI

1S/CH4O3S.Ag/c1-5(2,3)4;/h1H3,(H,2,3,4);/q;+1/p-1

InChI key

MLKQJVFHEUORBO-UHFFFAOYSA-M

Application

Catalyst for:
  • Heterocyclization reactions
  • CO2-mediated rearrangement of propargyl alcohols for the synthesis of a,β-unsaturated ketones and esters


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library


Articles

Access gold precatalysts, silver salts, and unsaturated building blocks to accelerate research success in catalysis applications.


Benedetto Natalini et al.
Talanta, 85(3), 1392-1397 (2011-08-03)
The successful enantioseparation of five 6-desfluoroquinolones with three polysaccharide-based stationary phases (namely, the cellulose-based Chiralpak IB and the two amylose-based Chiralpak AD-H and Lux Amylose-2) is herein described. The investigated species differ for the nature of substituents and/or the position
Neal W Sach et al.
Organic letters, 14(15), 3886-3889 (2012-07-18)
A general synthesis of aryl ethers from primary and secondary alcohols and aryl mesylates is presented. The reaction proceeds via a sulfonyl-transfer mechanism. In this paper, we compare the sulfonyl transfer reaction to Mitsunobu ether formation. The reaction can be
Qingxin Lei et al.
Journal of food science, 75(7), C633-C640 (2011-05-04)
Application of deuterium sulfide to powdered isolated soy proteins (ISP) was used to quench stable free radicals and produce a single deuterium label on amino acids where free radicals reside. The deuterium labels rendered increases of isotope ratio for the



Global Trade Item Number

SKUGTIN
550256-25G04061833548301
550256-5G04061833373422