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Molecule
ID:9358
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₆Cl₂O₂
Molecular Mass
205.03804
Exact Mass
203.97448479
Charge
0
InChI
InChI=1S/C8H6Cl2O2/c9-6-2-1-3-7(10)5(6)4-8(11)12/h1-3H,4H2,(H,11,12)
InChIKey
SFAILOOQFZNOAU-UHFFFAOYSA-N
Canonic Smiles
OC(=O)Cc1c(Cl)cccc1Cl
Isomeric Smiles
Clc1c(c(ccc1)Cl)CC(=O)O
Calculated Properties
JChem
Acid pKa
3.3143814
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
0.64988476
LogD (pH = 7.4)
-0.60393155
Log P
2.8190835
Molar Refractivity
46.9752
Polarizability
18.37317
Polar Surface Area
37.3
Rotatable Bonds
2
Lipinski's Rule of Five
true
Data Source
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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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General Information
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RDKit
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IUPAC name
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MP Biomedicals
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR6814
MP Biomedicals
05214185
Matrix Scientific
005575
Sigma Aldrich
259241
Bide Pharmatech
BD5855
Alfa Aesar
B21354
Academic Data
PubChem
81058
Names and Identifiers
IUPAC name
2-(2,6-dichlorophenyl)acetic acid
IUPAC Traditional name
(2,6-dichlorophenyl)acetic acid
Synonyms
2,6-Dichlorophenyl acetic acid 98%
2,6-DICHLOROPHENYL ACETIC ACID
2,6-Dichlorophenylacetic acid
2,6-二氯苯乙酸
2,6-Dichlorophenylacetic acid
Registration numbers
CAS Number
6575-24-2
MDL Number
MFCD00004320
PubChem SID
160972665
24855695
PubChem CID
81058
EC Number
229-504-0
Beilstein Number
1952744
Properties
Safety Information
MSDS Link
Download link
Source
Download link
Source
Download link
Source
TSCA Listed
false
Source
否
Source
Storage Warning
IRRITANT
Source
Irritant
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P280G-
P305+P351+P338
Source
German water hazard class
3
Source
European Hazard Symbols
Irritant (Xi)
Source
Risk Statements
36/37/38
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
Safety Statements
26
-
36
Source
26
-
37
Source
GHS Signal Word
Warning
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
Product Information
Purity
99%
Source
97%
Source
98%
Source
Certificate of Analysis
Download link
Source
Linear Formula
Cl2C6H3CH2CO2H
Source
Physical Property
Melting Point
158-161°C
Source
158-160°C
Source
158-161 °C(lit.)
Source
158-161°C
Source
Molecule Details
MP Biomedicals
05214185
MP Biomedicals Rare Chemical collection
Sigma Aldrich
259241
Packaging
25, 100 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
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