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2-Trifluoroacetylaminofluorene is a synthetic chemical compound with the molecular formula C14H8F3NO. It is a derivative of fluorene, a polycyclic aromatic hydrocarbon, and features a trifluoroacetyl group (CF3CO) attached to the amino group (NH2) at the 2-position of the fluorene ring. 2-TRIFLUOROACETYLAMINOFLUORENE is primarily used in research and development, particularly in the synthesis of various fluorinated organic compounds and as a building block for more complex molecules. Due to its unique structure and properties, 2-trifluoroacetylaminofluorene has potential applications in the fields of pharmaceuticals, agrochemicals, and materials science. However, it is important to handle 2-TRIFLUOROACETYLAMINOFLUORENE with care, as it may have toxic or hazardous properties.

363-17-7

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363-17-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 363-17-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,6 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 363-17:
(5*3)+(4*6)+(3*3)+(2*1)+(1*7)=57
57 % 10 = 7
So 363-17-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H10F3NO/c16-15(17,18)14(20)19-11-5-6-13-10(8-11)7-9-3-1-2-4-12(9)13/h1-6,8H,7H2,(H,19,20)

363-17-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(9H-fluoren-2-yl)-2,2,2-trifluoroacetamide

1.2 Other means of identification

Product number -
Other names N-9H-fluoren-2-yl-2,2,2-trifluoroacetamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:363-17-7 SDS

363-17-7Relevant academic research and scientific papers

Oxygen Sensitization of Electron Capture Response to Isomers of Polycyclic Aromatic Amines and Hydroxides

Campbell, J. A.,Grimsrud, E. P.,Hageman, L. R.

, p. 1335 - 1340 (2007/10/02)

The use of the oxygen-sensitized constant-current electron capture detector (ECD) with gas chromatography for analyte identification is extended by examining the responses of numerous polycyclic aromatic amines and hydroxides where an appropriate EC-enhancing chemical tag has been attached to the amino group or the hydroxy group has been methylated.For the majority of isomeric groups examined, measured response enhancements of the derivatives are sufficiently dependent on structural differences as to provide an additional means by which substitution isomers can be differentiated.The ion chemistry responsible for the EC and oxygen-sensitized responses also has been examined by the use of an atmospheric pressure ionization mass spectrometer (APIMS).

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