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Molecule
ID:9867
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₃H₈F₂O
Molecular Mass
218.1988264
Exact Mass
218.05432132
Charge
0
InChI
InChI=1S/C13H8F2O/c14-11-5-1-9(2-6-11)13(16)10-3-7-12(15)8-4-10/h1-8H
InChIKey
LSQARZALBDFYQZ-UHFFFAOYSA-N
Canonic Smiles
O=C(c1ccc(cc1)F)c1ccc(cc1)F
Isomeric Smiles
Fc1ccc(cc1)C(=O)c1ccc(cc1)F
Calculated Properties
JChem
H Acceptors
1
H Donor
0
LogD (pH = 5.5)
3.7180028
LogD (pH = 7.4)
3.7180028
Log P
3.7180028
Molar Refractivity
57.0663
Polarizability
21.3089
Polar Surface Area
17.07
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
No Data Available
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Molecule Details
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References
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Bioactivity
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Quote
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General Information
Calculated Properties
•
RDKit
•
JChem
Data Source
•
Commercial Catalog
•
Academic Data
Names and Identifiers
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IUPAC name
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Synonyms
•
IUPAC Traditional name
Registration numbers
Properties
•
Safety Information
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Product Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
•
Apollo Scientific
•
MP Biomedicals
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Wikipedia
•
Sigma Aldrich
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
PC2696
MP Biomedicals
05222946
Matrix Scientific
006464
Sigma Aldrich
115495
36914
Chemik
CHB85671
Enamine
EN300-118179
Alfa Aesar
A10653
Bide Pharmatech
BD33321
Academic Data
Wikipedia
4,4'-Difluorobenzophenone
PubChem
9582
Names and Identifiers
IUPAC name
bis(4-fluorophenyl)methanone
Synonyms
4,4'-Difluorobenzophenone
4,4'-二氟二苯甲酮
4,4′-Difluorobenzophenone
4,4'-Difluorobenzophenone 97%
Bis(4-fluorophenyl)methanone
4,4'-Difluorobenzophenone
bis(4-fluorophenyl)methanone
4,4'-二氟苯酮
IUPAC Traditional name
4,4'-difluorobenzophenone
Registration numbers
CAS Number
345-92-6
MDL Number
MFCD00000353
EC Number
206-466-3
Chemspider ID
9206
Beilstein Number
516231
PubChem SID
24847220
160973174
24862801
Wikipedia Title
4,4'-Difluorobenzophenone
PubChem CID
9582
Molecule Details
Apollo Scientific
PC2696
Intermediate for the manufacture of polyetheretherketone(PEEK) high performance polymer. Ask for reference.
MP Biomedicals
05222946
MP Biomedicals Rare Chemical collection
Wikipedia
4,4'-Difluorobenzophenone
Sigma Aldrich
115495
Packaging
25, 100 g in poly bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
MDL Number
•
EC Number
•
Chemspider ID
•
Beilstein Number
•
PubChem SID
•
Wikipedia Title
•
PubChem CID
Properties
Safety Information
Storage Warning
IRRITANT
Source
Irritant
Source
TSCA Listed
false
Source
否
Source
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Download link
Source
European Hazard Symbols
Irritant (Xi)
Source
RTECS
DJ0685000
Source
Risk Statements
R:
36/37/38
Source
36/37/38
Source
Safety Statements
S:
20
-
25
-
26
-
37/39
Source
26
-
37/39
Source
26
-
37
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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
GHS Signal Word
Warning
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
German water hazard class
3
Source
Product Information
Purity
99%
Source
≥99.0% (GC)
Source
95%
Source
98%
Source
98+%
Source
Certificate of Analysis
Download link
Source
Linear Formula
(FC6H4)2CO
Source
purum
Source
Physical Property
Melting Point
102-105°C
Source
102-110°C
Source
102°C
Source
107.5–108.5 °C
Source
102-105 °C(lit.)
Source
106-109 °C
Source
102 - 105°C
Source
106-110°C
Source
1.39
Source
>100°C
Source
170-172°C/10mm
Source
170-172°C/10mm
Source
Colorless Solid
Source
3.568
Source
Grade
Density
Flash Point
Boiling Point
Apperance
Hydrophobicity(logP)