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Molecule
ID:18467
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₃BrClN
Molecular Mass
216.46242
Exact Mass
214.91373878
Charge
0
InChI
InChI=1S/C7H3BrClN/c8-6-2-1-5(4-10)7(9)3-6/h1-3H
InChIKey
AYQBMZNSJPVADT-UHFFFAOYSA-N
Canonic Smiles
N#Cc1ccc(cc1Cl)Br
Isomeric Smiles
c1c(cc(c(c1)C#N)Cl)Br
Calculated Properties
JChem
H Acceptors
1
H Donor
0
LogD (pH = 5.5)
3.2021394
LogD (pH = 7.4)
3.2021394
Log P
3.2021394
Molar Refractivity
44.2072
Polarizability
16.95345
Polar Surface Area
23.79
Rotatable Bonds
0
Lipinski's Rule of Five
true
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Properties
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Related Proteins
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Molecular Spectra
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Molecule Details
暂无数据
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References
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Bioactivity
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General Information
Calculated Properties
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RDKit
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IUPAC name
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Synonyms
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IUPAC Traditional name
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Product Information
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From Data Sources
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PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR48257
Matrix Scientific
020603
Alfa Aesar
L10602
Chemik
CHB27431
Bide Pharmatech
BD18567
Academic Data
PubChem
7010420
Names and Identifiers
IUPAC name
4-bromo-2-chlorobenzonitrile
Synonyms
4-Bromo-2-chlorobenzonitrile
2-Chloro-4-bromobenzonitrile
4-Bromo-2-chlorobenzonitrile
4-溴-2-氯苯甲腈
IUPAC Traditional name
4-bromo-2-chlorobenzonitrile
Registration numbers
CAS Number
154607-01-9
PubChem SID
160981774
PubChem CID
7010420
MDL Number
MFCD00040883
Beilstein Number
3240885
Properties
Physical Property
Boiling Point
142-143°C
Source
142-143°C/10mm
Source
Melting Point
71-73°C
Source
67-72°C
Source
67-72°C
Source
Safety Information
MSDS Link
Download link
Source
TSCA Listed
false
Source
否
Source
Storage Warning
IRRITANT
Source
Toxic/Harmful/Irritant/Light Sensitive
Source
European Hazard Symbols
Harmful (X)
Source
Safety Statements
26
-
36/37
Source
Risk Statements
20/21/22
-
36/38
Source
Packing Group
III
Source
GHS Hazard statements
H311
-
H302
-
H332
-
H315
-
H319
Source
Hazard Class
6.1
Source
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
Source
GHS Precautionary statements
P280H-
P305+P351+P338
-
P309
-
P310
Source
UN Number
UN3439
Source
Product Information
Purity
97%
Source
96%
Source
References
PubChem Literature
No Data Available
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Bioactivity
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PubChem SID
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PubChem CID
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MDL Number
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Beilstein Number