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922722

Sigma-Aldrich

O-Pivaloylhydroxyamine triflic acid

Synonym(s):

2,2-dimethyl-, azanyl ester, 1,1,1-trifluoromethanesulfonate, PivONH3OTF, Propanoic acid

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About This Item

Empirical Formula (Hill Notation):
C5H11NO2 · CHF3O3S
CAS Number:
Molecular Weight:
267.22
UNSPSC Code:
12352106
NACRES:
NA.22

form

solid

Quality Level

Application

This hydroxylamine-based reagent enables the iron-catalyzed selective transformation of thiols to sulfinamides under mild conditions without the use of precious metal catalysts or additional oxidants. This reagent is shelf stable and facilitates the reaction in a single step and under mild conditions.

pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

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Sayanti Chatterjee et al.
Angewandte Chemie (International ed. in English), 60(2), 758-765 (2020-09-22)
An iron catalyzed reaction for the selective transformation of thiols (-SH) to sulfinamides (-SONH2 ) by a direct transfer of -O and free -NH2 groups has been developed. The reaction operates under mild conditions using a bench stable hydroxylamine derived

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