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Merck
CN

704083

三氟甲磺酸酐 溶液

1 M in methylene chloride

别名:

三氟甲烷磺酸酐 溶液

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关于此项目

经验公式(希尔记法):
C2F6O5S2
化学文摘社编号:
分子量:
282.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352101
MDL number:
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产品名称

三氟甲磺酸酐 溶液, 1 M in methylene chloride

InChI

1S/C2F6O5S2/c3-1(4,5)14(9,10)13-15(11,12)2(6,7)8

SMILES string

FC(F)(F)C(=O)OC(=O)C(F)(F)F

InChI key

WJKHJLXJJJATHN-UHFFFAOYSA-N

form

liquid

concentration

1 M in methylene chloride

refractive index

n20/D 1.402

density

1.359 g/mL at 25 °C

functional group

fluoro
triflate

storage temp.

2-8°C

Quality Level

Application

Catalyst for synthesis of Bacteroides fragilis zwitterionic polysaccharide Ai tetrasaccharide repeating unit via glycosylation

Reagent for stereoselective synthesis of mennosazide methyl uronate donors

Activator for direct glycosylation with anomeric hydroxy sugars
Trifluoromethanesulfonic anhydride solution is generally used to convert hydroxyl groups to triflic esters. It can be used to prepare triflic azide for azido amino acid synthesis.

signalword

Danger

Hazard Classifications

Carc. 2 - Eye Dam. 1 - Ox. Liq. 2 - Skin Corr. 1B - STOT SE 3

target_organs

Central nervous system, Respiratory system

存储类别

5.1B - Oxidizing hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

危险化学品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Building units for N-backbone cyclic peptides. 2. Synthesis of protected N-(ω-thioalkylene) amino acids and their incorporation into dipeptide units.
Bilan G and Gilon C
Tetrahedron, 51(38), 10513-10522 (1995)
Inhibiting EGFR dimerization using triazolyl-bridged dimerization arm mimics
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Tatsuya Higashi et al.
Journal of pharmaceutical and biomedical analysis, 117, 155-162 (2015-09-12)
The analysis of changes in the brain neurosteroid (NS) levels due to various stimuli can contribute to the elucidation of their physiological roles, and the discovery and development of new antipsychotic agents targeting neurosteroidogenesis. We developed methods for the differential
Surendra Vutti et al.
Chembiochem : a European journal of chemical biology, 16(5), 782-791 (2015-03-05)
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