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Molecule
ID:7076
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₇F₄N
Molecular Mass
193.1414928
Exact Mass
193.05146211
Charge
0
InChI
InChI=1S/C8H7F4N/c9-6-2-1-5(4-13)7(3-6)8(10,11)12/h1-3H,4,13H2
InChIKey
BLQGRYYLPWCHMA-UHFFFAOYSA-N
Canonic Smiles
NCc1ccc(cc1C(F)(F)F)F
Isomeric Smiles
c1c(cc(c(c1)CN)C(F)(F)F)F
Calculated Properties
JChem
H Acceptors
1
H Donor
1
LogD (pH = 5.5)
-0.82200044
LogD (pH = 7.4)
0.37263218
Log P
2.1195648
Molar Refractivity
40.7215
Polarizability
14.669819
Polar Surface Area
26.02
Rotatable Bonds
2
Lipinski's Rule of Five
true
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
No Data Available
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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General Information
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RDKit
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IUPAC name
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IUPAC Traditional name
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PubChem SID
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PubChem CID
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Physical Property
Related Proteins
Molecular Spectra
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TRC
References
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From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
001983
Apollo Scientific
PC4374Y
TRC
F595960
Enamine
EN300-40141
Chemik
CHB58003
Alfa Aesar
B20469
Academic Data
PubChem
2734878
Names and Identifiers
IUPAC name
[4-fluoro-2-(trifluoromethyl)phenyl]methanamine
IUPAC Traditional name
[4-fluoro-2-(trifluoromethyl)phenyl]methanamine
Synonyms
4-Fluoro-2-(trifluoromethyl)benzylamine
4-Fluoro-2-(trifluoromethyl)benzylamine 97%
4-fluoro-2-trifluoromethylbenzyl amine
1-[4-fluoro-2-(trifluoromethyl)phenyl]methanamine
[4-Fluoro-2-(trifluoromethyl)benzyl]amine
[[4-Fluoro-2-(trifluoromethyl)phenyl]methyl]amine
4-氟-2-三氟甲基苄胺
4-Fluoro-2-(trifluoromethyl)benzenemethanamine
4-Fluoro-2-(trifluoromethyl)benzylamine
Registration numbers
CAS Number
202522-22-3
MDL Number
MFCD00061164
PubChem SID
160970383
PubChem CID
2734878
Molecule Details
TRC
F595960
Used for preparation of heterocycle-substituted amide derivatives as ACAT inhibitors for pharmaceuticals compositions.
References
PubChem Literature
From Data Sources
•
Kinney, et al.: J. Med. Chem., 35, 4720 (1992)
•
Cerecetto, H., et al.: J. Agric. Food Chem., 48, 2995 (1992)
Bioactivity
PubChem BioAssay
Properties
Safety Information
Storage Warning
IRRITANT
Source
Corrosive/Store under nitrogen
Source
Air Sensitive
Source
MSDS Link
Download link
Source
Download link
Source
TSCA Listed
false
Source
否
Source
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
34
Source
8
Source
P260
-
P303+P361+P353
-
P305+P351+P338
-
P301+P330+P331
-
P405
-P501A
Source
20
-
23
-
26
-
36/37/39
-
45
Source
Corrosive (C)
III
Source
H314
-
H318
Source
UN2735
Source
Product Information
97%
Source
95%
Source
Download link
Source
Physical Property
1.453
Source
1.4530
Source
2.12
Source
Source
Source
GHS Pictograms
Risk Statements
Hazard Class
GHS Precautionary statements
Safety Statements
European Hazard Symbols
Packing Group
GHS Hazard statements
UN Number
Purity
Certificate of Analysis
Refractive Index
Hydrophobicity(logP)