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Molecule
ID:7667
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₄ClFO
Molecular Mass
158.5574632
Exact Mass
157.99347065
Charge
0
InChI
InChI=1S/C7H4ClFO/c8-6-2-1-3-7(9)5(6)4-10/h1-4H
InChIKey
OACPOWYLLGHGCR-UHFFFAOYSA-N
Canonic Smiles
O=Cc1c(F)cccc1Cl
Isomeric Smiles
c1(c(cccc1F)Cl)C=O
Calculated Properties
JChem
H Acceptors
1
H Donor
0
LogD (pH = 5.5)
2.4324949
LogD (pH = 7.4)
2.4324949
Log P
2.4324949
Molar Refractivity
37.6632
Polarizability
13.868247
Polar Surface Area
17.07
Rotatable Bonds
1
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
Calculated Properties
•
RDKit
•
JChem
Data Source
•
Commercial Catalog
•
Academic Data
Names and Identifiers
•
Synonyms
•
IUPAC name
•
IUPAC Traditional name
Registration numbers
Properties
Related Proteins
Molecular Spectra
Molecule Details
•
Sigma Aldrich
•
TRC
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
PC1828E
Matrix Scientific
002774
InterBioScreen
BB_SC-4834
Sigma Aldrich
141240
24615
TRC
C366280
C366285
Chemik
CHB20900
Bide Pharmatech
BD10270
Alfa Aesar
A10513
Academic Data
PubChem
67847
Names and Identifiers
Synonyms
2-Chloro-6-fluorobenzaldehyde
2-氯-6-氟苯甲醛
2-Chloro-6-fluorobenzaldehyde
2-Chloro-6-fluorobenzaldehyde 97%
2-Fluoro-6-chlorobenzaldehyde
5-Chloro-2-fluorobenzoic Acid
5-Chloro-2-fluoro-benzoic Acid
2-Fluoro-5-chlorobenzoic Acid
IUPAC name
2-chloro-6-fluorobenzaldehyde
IUPAC Traditional name
2-chloro-6-fluorobenzaldehyde
Registration numbers
MDL Number
MFCD00003306
EC Number
206-860-5
Beilstein Number
2245530
PubChem SID
24854788
24848497
160970974
CAS Number
387-45-1
394-30-9
PubChem CID
67847
Molecule Details
Sigma Aldrich
141240
Packaging
25, 100 g in glass bottle
TRC
C366285
Used in the synthesis of some new pyridine-2,6-carboxamide-derived Schiff bases as potential antimicrobial agents.
References
PubChem Literature
From Data Sources
•
Karthikeyan, M., et al.: Bioorg. Med. Chem., 14, 7482 (2006)
•
Fakhr, I., et al.: Arch. Pharm. Chem. Life Sci., 341, 174 (2006)
•
Bayrak, H., et al.: Eur. J. Med. Chem., 44, 1057 (2006)
Bioactivity
PubChem BioAssay
Registration numbers
•
MDL Number
•
EC Number
•
Beilstein Number
•
PubChem SID
•
CAS Number
•
PubChem CID
Properties
•
Physical Property
•
Product Information
•
Safety Information
Properties
Physical Property
Boiling Point
91-93°C/10mm
Source
91-93°C/10mm
Source
Melting Point
35-38°C
Source
32-39°C
Source
32-35 °C(lit.)
Source
32-35 °C
Source
145-147°C
Source
35-39°C
Source
101°C
Source
102 °C
Source
215.6 °F
Source
101°C(213°F)
Source
DMSO
Source
Methanol
Source
White Solid
Source
Product Information
97%
Source
95%
Source
≥90% (GC)
Source
ClC6H3(F)CHO
Source
technical
Source
Download link
Source
Safety Information
Download link
Source
Download link
Source
Download link
Source
Download link
Source
IRRITANT
Source
Irritant/Air Sensitive/Store under Argon
Source
Air Sensitive
Source
TSCA Listed
true
Source
是
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
Risk Statements
36/37/38
Source
Safety Statements
26
-
37/39
Source
26
-
37
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
European Hazard Symbols
Irritant (Xi)
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
GHS Signal Word
Warning
Source
German water hazard class
1
Source
Storage Condition
Refrigerator
Source
Flash Point
Solubility
Apperance
Purity
Linear Formula
Grade
Certificate of Analysis
MSDS Link
Storage Warning