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Merck
CN

688916

N-[(2R)-2-吡咯烷甲基]-三氟甲磺酰胺

≥98.5% (T)

别名:

1,1,1-三氟-N-[(2R)-2-吡咯烷甲基]-甲磺酰胺

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关于此项目

经验公式(希尔记法):
C6H11F3N2O2S
化学文摘社编号:
分子量:
232.22
PubChem Substance ID:
UNSPSC Code:
12352005
Beilstein/REAXYS Number:
10255865
MDL number:
Assay:
≥98.5% (T)
Form:
powder
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SMILES string

FC(F)(F)S(=O)(=O)NC[C@H]1CCCN1

InChI

1S/C6H11F3N2O2S/c7-6(8,9)14(12,13)11-4-5-2-1-3-10-5/h5,10-11H,1-4H2/t5-/m1/s1

InChI key

RIWFUAUXWIEOTK-RXMQYKEDSA-N

assay

≥98.5% (T)

form

powder

optical activity

[α]/D -13±1°, c = 1% in methanol

optical purity

ee: ≥98.0%

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

法规信息

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历史批次信息供参考:

分析证书(COA)

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Liansuo Zu et al.
Organic letters, 10(6), 1211-1214 (2008-02-15)
Fluorous (S) pyrrolidine sulfonamide serves as an efficient promoter for highly enantioselective aldol reactions of ketones and aldehydes with aromatic aldehydes on water. A notable feature of the organocatalyst is that it can be recovered from the reaction mixtures by
Direct, highly enantioselective pyrrolidine sulfonamide catalyzed Michael addition of aldehydes to nitrostyrenes.
Wei Wang et al.
Angewandte Chemie (International ed. in English), 44(9), 1369-1371 (2005-01-25)
Liansuo Zu et al.
Organic letters, 8(14), 3077-3079 (2006-06-30)
[reaction: see text] A recycle and reusable fluorous (S)-pyrrolidine sulfonamide organocatalyst has been developed for promoting highly enantio- and diastereoselective Michael addition reactions of ketones and aldehydes with nitroolefins in water. The organocatalyst is conveniently recovered from the reaction mixtures

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