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Molecule
ID:78343
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₃H₉Cl₂NO
Molecular Mass
266.12266
Exact Mass
265.00611927
Charge
0
InChI
InChI=1S/C13H9Cl2NO/c14-8-5-6-12(16)10(7-8)13(17)9-3-1-2-4-11(9)15/h1-7H,16H2
InChIKey
KWZYIAJRFJVQDO-UHFFFAOYSA-N
Canonic Smiles
Clc1ccc(c(c1)C(=O)c1ccccc1Cl)N
Isomeric Smiles
O=C(c1cc(ccc1N)Cl)c1c(cccc1)Cl
Calculated Properties
JChem
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
4.4617014
LogD (pH = 7.4)
4.4617615
Log P
4.4617624
Molar Refractivity
70.9435
Polarizability
26.859924
Polar Surface Area
43.09
Rotatable Bonds
2
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
•
Academic Data
Names and Identifiers
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IUPAC name
•
Synonyms
•
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
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Sigma Aldrich
•
TRC
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR18295
Sigma Aldrich
105155
TRC
A604630
Alfa Aesar
B20360
Academic Data
PubChem
18069
Names and Identifiers
IUPAC name
4-chloro-2-(2-chlorobenzoyl)aniline
Synonyms
2-Amino-2',5-dichlorobenzophenone 99%
Lorazepam IMP A
2,5'-Dichloro-2'-aminobenzophenone
NSC 611905
(2-Amino-5-chlorophenyl)(2-chlorophenyl)-methanone
2-Amino-5-chloro-2'-chlorobenzophenone
2',5-Dichloro-2-aminobenzophenone
2-Amino-2',5-dichlorobenzophenone
2-氨基-2',5-二氯苯并苯酮
2-Amino-2',5-dichlorobenzophenone
2-Amino-2′,5-dichlorobenzophenone
2-氨基-2′,5-二氯苯甲酮
IUPAC Traditional name
4-chloro-2-(2-chlorobenzoyl)aniline
Registration numbers
PubChem CID
18069
PubChem SID
162043112
24846691
MDL Number
MFCD00007840
EC Number
220-985-2
CAS Number
2958-36-3
Beilstein Number
652774
Molecule Details
Sigma Aldrich
105155
Packaging
10, 50 g in glass bottle
TRC
A604630
Lorazepam Impurity A.
References
PubChem Literature
From Data Sources
•
Herman, R.J., et al.: Clin. Pharmacol. Ther., 46, 18 (1989)
•
Koves, E.M., et al.: J. Anal. Toxicol., 13, 69 (1989)
Bioactivity
PubChem BioAssay
Registration numbers
•
PubChem CID
•
PubChem SID
•
MDL Number
•
EC Number
•
CAS Number
•
Beilstein Number
Properties
Safety Information
Storage Warning
Harmful/Irritant
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
H301
-
H315
-
H319
-
H335
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P261
-
P301+P310
-
P305+P351+P338
-
P302+P352
-
P405
-P501A
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
Risk Statements
36/37/38
Source
22
-
36/37/38
Source
Safety Statements
26
-
37/39
Source
26
-
36/37
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
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
GHS Signal Word
Warning
Source
MSDS Link
Download link
Source
Download link
Source
RTECS
DJ0200000
Source
European Hazard Symbols
Irritant (Xi)
Source
Harmful (X)
German water hazard class
3
Source
Storage Condition
Refrigerator
Source
TSCA Listed
是
Source
Physical Property
Melting Point
87-89°C
Source
87-89 °C(lit.)
Source
87-89°C
Source
Apperance
Yellow Solid
Source
Solubility
Methanol
Source
DMSO
Source
Product Information
Purity
99%
Source
Linear Formula
H2NC6H3(Cl)COC6H4Cl
Source
Certificate of Analysis
Download link
Source
Source
Source