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Molecule
ID:77589
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₅ClN₂
Molecular Mass
152.581
Exact Mass
152.01412585
Charge
0
InChI
InChI=1S/C7H5ClN2/c8-6-2-1-5(4-9)7(10)3-6/h1-3H,10H2
InChIKey
UZHALXIAWJOLLR-UHFFFAOYSA-N
Canonic Smiles
N#Cc1ccc(cc1N)Cl
Isomeric Smiles
Clc1cc(c(cc1)C#N)N
Calculated Properties
JChem
Acid pKa
19.38079
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
1.6044185
LogD (pH = 7.4)
1.6044602
Log P
1.6044607
Molar Refractivity
41.2848
Polarizability
15.175691
Polar Surface Area
49.81
Rotatable Bonds
0
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
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Commercial Catalog
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Academic Data
Names and Identifiers
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Synonyms
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IUPAC Traditional name
•
IUPAC name
Registration numbers
Properties
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
References
•
PubChem Literature
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From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR15043
Sigma Aldrich
405280
07385
Chemik
CHB27611
Alfa Aesar
B25120
Bide Pharmatech
BD4363
Academic Data
PubChem
170059
Names and Identifiers
Synonyms
5-Chloro-2-cyanoaniline
2-氨基-4-氯苄腈
2-Amino-4-chlorobenzonitrile
5-氯-2-氰基苯胺
4-氯邻氨基苯腈
4-Chloroanthranilonitrile
2-氨基-4-氯苯甲腈
2-Amino-4-chlorobenzonitrile
4-Chloro-2-aminobenzonitrile
IUPAC Traditional name
2-amino-4-chlorobenzonitrile
IUPAC name
2-amino-4-chlorobenzonitrile
Registration numbers
CAS Number
38487-86-4
MDL Number
MFCD00035927
Beilstein Number
2085559
PubChem SID
24865306
162042461
EC Number
253-967-8
PubChem CID
170059
Molecule Details
Sigma Aldrich
405280
Packaging
10, 50 g in glass bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
MDL Number
•
Beilstein Number
•
PubChem SID
•
EC Number
•
PubChem CID
Properties
•
Safety Information
•
Physical Property
•
Product Information
Properties
Safety Information
Storage Warning
Irritant/Light Sensitive/Keep Cold
Source
MSDS Link
Download link
Source
Download link
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P261
-
P301+P310
-
P305+P351+P338
-
P361
-
P405
-P501A
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
H315
-
H319
-
H335
Source
H301
-
H311
-
H332
-
H315
-
H319
-
H335
Source
36/37/38
Source
20/21/22
-
36/37/38
Source
26
-
36
Source
26
-
36/37
Source
Warning
Source
Irritant (Xi)
3
Source
6.1
Source
是
Source
III
Source
UN3439
Source
Physical Property
157-162°C
Source
157-162 °C(lit.)
Source
157-162 °C
Source
159-162°C
Source
Product Information
99%
Source
≥97.0% (HPLC)
Source
97%
Source
H2NC6H3(Cl)CN
Source
purum
Source
Source
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
Source
Source
Harmful (X)
Source
GHS Pictograms
GHS Hazard statements
Risk Statements
Safety Statements
GHS Signal Word
European Hazard Symbols
German water hazard class
Hazard Class
TSCA Listed
Packing Group
UN Number
Melting Point
Purity
Linear Formula
Grade