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007272

007272-1g



Silver trifluoromethanesulfonate


CAS Number: 2923-28-6
   
Molecular Formula: CAgF3O3S
   
Molecular Weight: 256.94
   
MDL Number: MFCD00013226


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007272-1g
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007272-5g
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007272-10g
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007272-25g
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007272-50g
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007272-100g
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007272-500g
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Purity:99%
Mp:286°
 
Pictograms:
Signal Word:Warning
Hazard Statements:H302, H315, H319, H335
Precautionary Statements:P261, P301 + P312, P302 + P352, P304 + P340, P305 + P351 + P338
Risk Statements:36/37/38
Safety Statements:22-24/25-26-28-36/37/39
SDS: See MSDS
 

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A halide abstraction reagent applied in the etherification of alcohols with primary alkyl halides,1 and generation of cationic rhodium catalysts from chlororhodium complexes for the hydrophosphination of acetylenes.2 Also employed as a catalyst for the preparation of silyl ethers by hydrosilylation of aldehydes,3  synthesis of 1-(isoquinolin-1-yl)guanidines via a three-component reaction of 2-alkynylbenzaldehyde, sulfonohydrazide, with carbodiimide,4 cyclization of enynals or enynones with amines,5 cyclopropenation of internal alkynes using donor-/acceptor-substituted diazo compounds as carbenoid precursors,5 reaction of 2-Alkynylbenzaldoxime with amine to afford 1-aminoisoquinolines,6 cycloisomerization of a variety of allenynamides,7 and the cross-dehydrogenative-coupling of terminal aromatic alkynes and benzylic ethers.8 

Reference

1.        Tetrahedron Lett. 199435, 8111.
2.        J. Org. Chem. 200671, 9248.
3.        Chem. Commun. 2006, 1359.
4.        Tetrahedron 201167, 5871.
5.        ARKIVOC 2011, 381.
6.        Org. Lett. 201113, 3984.
7.        Org. Biomol. Chem. 20119, 4763.
8.        Org. Lett. 201113, 2952.
9.        Heterocycles 201082, 555.

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