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Molecule
ID:10574
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₅BCl₂O₂
Molecular Mass
190.8197
Exact Mass
189.97596516
Charge
0
InChI
InChI=1S/C6H5BCl2O2/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3,10-11H
InChIKey
JKIGHOARKAIPJI-UHFFFAOYSA-N
Canonic Smiles
OB(c1ccc(c(c1)Cl)Cl)O
Isomeric Smiles
c1c(c(cc(c1)B(O)O)Cl)Cl
Calculated Properties
JChem
Acid pKa
8.652279
H Acceptors
2
H Donor
2
LogD (pH = 5.5)
2.6754959
LogD (pH = 7.4)
2.652286
Log P
2.6758
Molar Refractivity
40.2131
Polarizability
17.376898
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
Calculated Properties
•
RDKit
•
JChem
Data Source
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Commercial Catalog
•
Academic Data
Names and Identifiers
•
Synonyms
•
IUPAC name
•
IUPAC Traditional name
Registration numbers
Properties
•
Safety Information
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Physical Property
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Product Information
Related Proteins
Molecular Spectra
Molecule Details
•
Sigma Aldrich
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR10445
Matrix Scientific
007404
Sigma Aldrich
471917
Chemik
CBC04400
Enamine
EN300-49160
Bide Pharmatech
BD3306
Alfa Aesar
B24292
A&J Pharmtech
AJA-O40344
Academic Data
PubChem
2734330
Names and Identifiers
Synonyms
3,4-Dichlorophenylboronic acid
3,4-Dichlorobenzeneboronic acid
(3,4-dichlorophenyl)boranediol
3,4-Dichlorophenylboronic acid
3,4-Dichlorobenzeneboronic acid
3,4-二氯苯硼酸
3,4-Dichlorobenzeneboronic acid
3,4-Dichlorophenylboronic acid
IUPAC name
(3,4-dichlorophenyl)boronic acid
IUPAC Traditional name
3,4-dichlorophenylboronic acid
Registration numbers
CAS Number
151169-75-4
MDL Number
MFCD01074646
PubChem SID
24870771
160973881
Beilstein Number
7369790
EC Number
000-000-0
PubChem CID
2734330
Properties
Safety Information
Storage Warning
IRRITANT
Source
Irritant/Store under Argon/Keep Cold
Source
MSDS Link
Download link
Source
Download link
Source
TSCA Listed
false
Source
否
Source
GHS Signal Word
Warning
Source
Safety Statements
26
-
36
Source
26
-
37
-
60
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
Risk Statements
36/37/38
Source
European Hazard Symbols
Irritant (Xi)
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 Precautionary statements
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
German water hazard class
3
Source
Physical Property
Melting Point
270-274°C
Source
280-285°C
Source
280-285 °C(lit.)
Source
280 - 285°C
Source
270-274°C
Source
Hydrophobicity(logP)
2.901
Source
Product Information
Purity
97%
Source
95%
Source
98%
Source
Linear Formula
Cl2C6H3B(OH)2
Source
Molecule Details
Sigma Aldrich
471917
Packaging
5, 25 g in glass bottle
Application
Reactant involved in:
• Lithiation/borylation-protodeboronation of homoallyl carbamates1
• Suzuki coupling reactions2,3Precursor / reactant involved in synthesis of biologically active molecules including:
• Mycobacterium tuberculosis H37Rv chorismate mutase inhibitors2
• Pyrrole derivatives as PDE4B inhibitors3
• Nitrovinyl biphenyls as anticancer agents4
• Dual immunosuppressive and anti-inflammatory agents5
• Pyrazolopyrimidines as Cryptosporidium and Toxoplasma CDPK1 inhibitors6
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
MDL Number
•
PubChem SID
•
Beilstein Number
•
EC Number
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PubChem CID