제품 이름
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
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
저장 등급
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
문서
Access gold precatalysts, silver salts, and unsaturated building blocks to accelerate research success in catalysis applications.
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
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
Solvejg Jørgensen et al.
Physical chemistry chemical physics : PCCP, 15(14), 5140-5150 (2013-03-02)
The gas phase reaction between methane sulfonic acid (CH3SO3H; MSA) and the hydroxyl radical (HO), without and with a water molecule, was investigated with DFT-B3LYP and CCSD(T)-F12 methods. For the bare reaction we have found two reaction mechanisms, involving proton
