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1-Trifluoroacetyl piperidine_Molecular_structure_CAS_340-07-8)
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1-Trifluoroacetyl piperidine

Catalog No. 683035 Name Sigma Aldrich
CAS Number 340-07-8 Website http://www.sigmaaldrich.com
M. F. C7H10F3NO Telephone 1-800-521-8956
M. W. 181.1556096 Fax
Purity 97% Email
Storage Chembase ID: 141154

SYNONYMS

Title
1-三氟乙酰基哌啶
IUPAC name
2,2,2-trifluoro-1-(piperidin-1-yl)ethan-1-one
IUPAC Traditional name
2,2,2-trifluoro-1-(piperidin-1-yl)ethanone
Synonyms
2,2,2-Trifluoro-1-(piperidin-1-yl)ethanone

DATABASE IDS

MDL Number MFCD00466213
PubChem SID 24885744
CAS Number 340-07-8

PROPERTIES

Empirical Formula (Hill Notation) C7H10F3NO
Purity 97%
Density 1.226 g/mL at 25 °C
Flash Point 76 °C
Flash Point 168.8 °F
Refractive Index n20/D 1.4171
GHS Pictograms GHS06
GHS Pictograms GHS09
GHS Signal Word Danger
GHS Hazard statements H300-H319-H400
European Hazard Symbols Toxic Toxic (T)
MSDS Link Download
Personal Protective Equipment Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Precautionary statements P264-P273-P301 + P310-P305 + P351 + P338
RID/ADR UN 2810 6.1/PG 3
Risk Statements 25-50
Safety Statements 45-61
Hazard Class 6.1
UN Number 2810
Packing Group 3
German water hazard class 3

DETAILS

Description (English)
Packaging
5, 25 g in glass bottle
Application
Reactant for synthesis of:
• Photoreactive probes that differentiate the binding sites of noncompetitive GABA receptor antagonists1
• Photoactive a-mannosides and mannosyl peptides2
• Inactivators of human cytochrome P450 2B63
• Photoaffinity labeled fusidic acid analogues4
• Hydroxyamides as anticonvulsants5
• ET-18-OCH3 with antiproliferative properties6
Description (简体中文)
包装
5, 25 g in glass bottle
Application
Reactant for synthesis of:
• Photoreactive probes that differentiate the binding sites of noncompetitive GABA receptor antagonists1
• Photoactive a-mannosides and mannosyl peptides2
• Inactivators of human cytochrome P450 2B63
• Photoaffinity labeled fusidic acid analogues4
• Hydroxyamides as anticonvulsants5
• ET-18-OCH3 with antiproliferative properties6

REFERENCES