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Molecule
ID:78358
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₇ClO
Molecular Mass
154.59358
Exact Mass
154.01854252
Charge
0
InChI
InChI=1S/C8H7ClO/c1-6(10)7-3-2-4-8(9)5-7/h2-5H,1H3
InChIKey
UUWJBXKHMMQDED-UHFFFAOYSA-N
Canonic Smiles
Clc1cccc(c1)C(=O)C
Isomeric Smiles
O=C(c1cc(ccc1)Cl)C
Calculated Properties
JChem
Acid pKa
15.949947
H Acceptors
1
H Donor
0
LogD (pH = 5.5)
2.134938
LogD (pH = 7.4)
2.134938
Log P
2.134938
Molar Refractivity
41.2656
Polarizability
15.928728
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
Names and Identifiers
•
Synonyms
•
IUPAC Traditional name
•
IUPAC name
Registration numbers
Properties
•
Physical Property
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Safety Information
•
Product Information
Related Proteins
Molecular Spectra
Molecule Details
•
Sigma Aldrich
References
Bioactivity
Names and Identifiers
Synonyms
3'-Chloroacetophenone 98+%
1-(3-Chlorophenyl)ethan-1-one
3′-Chloroacetophenone
3′-氯苯乙酮
3'-氯苯乙酮
3'-Chloroacetophenone
1-(3-Chlorophenyl)ethanone
IUPAC Traditional name
M-chloroacetophenone
IUPAC name
1-(3-chlorophenyl)ethan-1-one
Registration numbers
MDL Number
MFCD00000593
Beilstein Number
636318
CAS Number
99-02-5
EC Number
202-721-8
PubChem SID
162043127
24857361
24853686
PubChem CID
14933
Molecule Details
Sigma Aldrich
288799
Packaging
5, 25 g in glass bottle
Registration numbers
•
MDL Number
•
Beilstein Number
•
CAS Number
•
EC Number
•
PubChem SID
•
PubChem CID
Properties
Physical Property
Boiling Point
227-229°C
Source
227-229 °C(lit.)
Source
227-229°C
Source
Density
1.191
Source
1.191 g/mL at 25 °C(lit.)
Source
Flash Point
105°C
Source
221 °F
Source
105 °C
Source
105°C(221°F)
Source
1.5506
Source
n20/D 1.550(lit.)
Source
n20/D 1.550
Source
Safety Information
Toxic/Harmful/Irritant/Lachrymatory
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
Product Information
ClC6H4COCH3
Source
98%
Source
≥97.0% (GC)
Source
98+%
Source
purum
Source
Data Source
Commercial Catalog
Apollo Scientific
OR18322
Sigma Aldrich
288799
22845
Bide Pharmatech
BD41049
Alfa Aesar
A15592
Academic Data
PubChem
14933
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Data Source
•
Commercial Catalog
•
Academic Data
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Source
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P261
-
P301+P310
-
P305+P351+P338
-
P302+P352
-
P405
-P501A
Source
Safety Statements
26
-
36
Source
26
-
36/37
Source
UN Number
3416
Source
UN3416
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
H301
-
H315
-
H319
-
H335
Source
German water hazard class
3
Source
Packing Group
2
Source
II
Source
European Hazard Symbols
Irritant (Xi)
Source
Harmful (X)
Personal Protective Equipment
Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
Source
RID/ADR
UN 3416 6.1/PG 2
Source
MSDS Link
Download link
Source
Download link
Source
Hazard Class
6.1
Source
GHS Signal Word
Warning
Source
Risk Statements
36/37/38
Source
22
-
36/37/38
Source
TSCA Listed
是
Source
Refractive Index
Storage Warning
GHS Pictograms
Linear Formula
Purity
Grade
Source