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Molecule
ID:34859
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₃F₅N₂
Molecular Mass
198.093436
Exact Mass
198.02163921
Charge
0
InChI
InChI=1S/C6H3F5N2/c7-1-2(8)4(10)6(13-12)5(11)3(1)9/h13H,12H2
InChIKey
BYCUWCJUPSUFBX-UHFFFAOYSA-N
Canonic Smiles
NNc1c(F)c(F)c(c(c1F)F)F
Isomeric Smiles
c1(c(c(c(c(c1F)F)F)F)F)NN
Calculated Properties
JChem
Acid pKa
11.822388
H Acceptors
2
H Donor
2
LogD (pH = 5.5)
2.0568798
LogD (pH = 7.4)
2.0781043
Log P
2.078398
Molar Refractivity
36.8467
Polarizability
12.154789
Polar Surface Area
38.05
Rotatable Bonds
1
Lipinski's Rule of Five
true
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Registration numbers
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Properties
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Related Proteins
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Molecular Spectra
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Molecule Details
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Bioactivity
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General Information
Calculated Properties
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RDKit
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IUPAC name
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IUPAC Traditional name
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Molecular Spectra
Molecule Details
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
037626
Apollo Scientific
PC5690
Sigma Aldrich
156388
76752
Alfa Aesar
A13302
Academic Data
PubChem
13236
Names and Identifiers
IUPAC name
(pentafluorophenyl)hydrazine
IUPAC Traditional name
(pentafluorophenyl)hydrazine
Synonyms
(Pentafluorophenyl)hydrazine
Perfluorophenylhydrazine 97%
Pentafluorophenylhydrazine
五氟苯肼
Pentafluorophenylhydrazine
Registration numbers
CAS Number
828-73-9
MDL Number
MFCD00007574
EC Number
212-586-7
Beilstein Number
747800
PubChem SID
24887048
24849610
160998166
PubChem CID
13236
Properties
Safety Information
Storage Warning
IRRITANT
Source
Irritant
Source
Air Sensitive
Source
TSCA Listed
false
Source
否
Source
MSDS Link
Download link
Source
Download link
Source
Download link
Source
GHS Signal Word
Warning
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
German water hazard class
3
Source
Risk Statements
36/37/38
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
European Hazard Symbols
Irritant (Xi)
Source
RTECS
MV8325000
Source
Safety Statements
26
-
36
Source
26
-
37
Source
Physical Property
Melting Point
74-76°C
Source
74-76 °C(lit.)
Source
75-79 °C
Source
73-78°C
Source
Product Information
Purity
97%
Source
≥95.0% (GC)
Source
Linear Formula
C6F5NHNH2
Source
Grade
purum
Source
Molecule Details
Sigma Aldrich
156388
Packaging
10 g in glass bottle
76752
Caution
may discolor to orange-brown on storage
References
PubChem Literature
From Data Sources
•
Reagent for the derivatization of ketones for GC electron-capture detection:
Anal. Biochem
,
20
, 394 (1967).
Bioactivity
PubChem BioAssay
Registration numbers
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CAS Number
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MDL Number
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EC Number
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Beilstein Number
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PubChem SID
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PubChem CID