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Molecule
ID:32901
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₅BClFO₂
Molecular Mass
174.3651032
Exact Mass
174.0055157
Charge
0
InChI
InChI=1S/C6H5BClFO2/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3,10-11H
InChIKey
GGTUVWGMCFXUAS-UHFFFAOYSA-N
Canonic Smiles
Clc1ccc(c(c1)B(O)O)F
Isomeric Smiles
c1(c(ccc(c1)Cl)F)B(O)O
Calculated Properties
JChem
Acid pKa
8.0928755
H Acceptors
2
H Donor
2
LogD (pH = 5.5)
2.2961986
LogD (pH = 7.4)
2.2174644
Log P
2.2973
Molar Refractivity
35.6247
Polarizability
15.177813
Polar Surface Area
40.46
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
No Data Available
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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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IUPAC name
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CAS Number
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MDL Number
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PubChem CID
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Molecular Spectra
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
035639
Apollo Scientific
PC1635
Sigma Aldrich
557234
Alfa Aesar
H53108
A&J Pharmtech
AJA-O32585
Academic Data
PubChem
3718925
Names and Identifiers
Synonyms
5-Chloro-2-fluorophenylboronic acid
5-氯-2-氟苯硼酸
5-Chloro-2-fluorobenzeneboronic acid 97%
5-Chloro-2-fluorophenylboronic acid
5-Chloro-2-fluorobenzeneboronic acid
5-Chloro-2-fluorophenylboronic acid
IUPAC name
(5-chloro-2-fluorophenyl)boronic acid
IUPAC Traditional name
5-chloro-2-fluorophenylboronic acid
Registration numbers
CAS Number
352535-83-2
MDL Number
MFCD05664225
PubChem CID
3718925
PubChem SID
160996208
24879654
Properties
Safety Information
MSDS Link
Download link
Source
Download link
Source
Storage Warning
IRRITANT
Source
Irritant
Source
TSCA Listed
false
Source
否
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
German water hazard class
3
Source
Risk Statements
36/37/38
Source
GHS Precautionary statements
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
Safety Statements
26
-
37
-
60
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 Hazard statements
H315
-
H319
-
H335
Source
European Hazard Symbols
Irritant (Xi)
Source
Physical Property
Melting Point
182-188°C
Source
122-127 °C(lit.)
Source
182-188°C
Source
Product Information
Linear Formula
ClC6H3(F)B(OH)2
Source
Purity
97%
Source
98%
Source
Molecule Details
Sigma Aldrich
557234
Other Notes
Contains varying amounts of anhydride
Packaging
5 g in glass bottle
Application
Reactant involved in:
• Suzuki cross-coupling reactions1
• Synthesis of biaryl amides with muscarinic acetylcholine receptor subtype M1 agonistic activity2
• Synthesis of kinesin spindle protein inhibitors3
• GABA α2/3 agonist preparation4
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay