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Molecule
ID:8350
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₆BClO₂
Molecular Mass
156.37464
Exact Mass
156.01493751
Charge
0
InChI
InChI=1S/C6H6BClO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4,9-10H
InChIKey
RRCMGJCFMJBHQC-UHFFFAOYSA-N
Canonic Smiles
OB(c1ccccc1Cl)O
Isomeric Smiles
Clc1c(B(O)O)cccc1
Calculated Properties
JChem
Acid pKa
8.407106
H Acceptors
2
H Donor
2
LogD (pH = 5.5)
2.1572654
LogD (pH = 7.4)
2.1172562
Log P
2.1578
Molar Refractivity
35.4083
Polarizability
15.423168
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
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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
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Academic Data
Names and Identifiers
Registration numbers
Properties
Related Proteins
Molecular Spectra
Molecule Details
•
Sigma Aldrich
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
003912
Apollo Scientific
OR3349
Maybridge
AC35899
Sigma Aldrich
445215
Chemik
CBC00128
Enamine
EN300-114510
Bide Pharmatech
BD3442
Alfa Aesar
B23324
A&J Pharmtech
AJA-O40050
Academic Data
PubChem
2734322
Registration numbers
EC Number
000-000-0
CAS Number
3900-89-8
MDL Number
MFCD00674012
Beilstein Number
3030414
PubChem SID
160971657
24868167
PubChem CID
2734322
Molecule Details
Sigma Aldrich
445215
Other Notes
Contains varying amounts of anhydride
Packaging
1, 5 g in glass bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
EC Number
•
CAS Number
•
MDL Number
•
Beilstein Number
•
PubChem SID
•
PubChem CID
Properties
•
Physical Property
•
Safety Information
•
Product Information
Properties
Physical Property
Melting Point
176-179°C
Source
92-102 °C(lit.)
Source
101 - 102°C
Source
ca 95-100°C
Source
Hydrophobicity(logP)
2.308
Source
Safety Information
MSDS Link
Download link
Source
Download link
Source
false
Source
否
Source
IRRITANT
Source
Irritant
Source
3
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
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
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
Irritant (Xi)
36/37/38
Source
H315
-
H319
-
H335
Source
26
-
37
Source
Product Information
97%
Source
≥95.0%
Source
95%
Source
98%
Source
ClC6H4B(OH)2
Source
Source
Source
TSCA Listed
Storage Warning
German water hazard class
Personal Protective Equipment
GHS Pictograms
GHS Precautionary statements
European Hazard Symbols
Risk Statements
GHS Hazard statements
Safety Statements
Purity
Linear Formula
Names and Identifiers
Synonyms
2-Chlorophenylboronic acid
2-Chlorobenzeneboronic acid
2-Chlorophenylboronic acid
2-Chlorobenzeneboronic acid
o-chloro-Benzeneboronic acid
2-氯苯基硼酸
(o-Chlorophenyl)boronic acid
2-Chlorobenzeneboronic acid
(2-chlorophenyl)boronic acid
2-Chlorophenylboronic acid
2-氯苯硼酸
IUPAC name
(2-chlorophenyl)boronic acid
IUPAC Traditional name
2-chlorophenylboronic acid
Names and Identifiers
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Synonyms
•
IUPAC name
•
IUPAC Traditional name