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Molecule
ID:64582
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₆BrN
Molecular Mass
208.05464
Exact Mass
206.9683612
Charge
0
InChI
InChI=1S/C9H6BrN/c10-8-5-6-11-9-4-2-1-3-7(8)9/h1-6H
InChIKey
SUXIPCHEUMEUSV-UHFFFAOYSA-N
Canonic Smiles
Brc1ccnc2c1cccc2
Isomeric Smiles
c12c(ccnc1cccc2)Br
Calculated Properties
JChem
H Acceptors
1
H Donor
0
LogD (pH = 5.5)
2.8964198
LogD (pH = 7.4)
2.8996122
Log P
2.8996532
Molar Refractivity
47.6021
Polarizability
19.613428
Polar Surface Area
12.89
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
No Data Available
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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
•
IUPAC name
•
IUPAC Traditional name
•
Synonyms
Registration numbers
•
PubChem CID
•
PubChem SID
•
MDL Number
•
CAS Number
Properties
•
Safety Information
•
Product Information
•
Physical Property
Related Proteins
Molecular Spectra
Molecule Details
•
Sigma Aldrich
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR8603
Sigma Aldrich
693944
Matrix Scientific
069910
Bide Pharmatech
BD95370
A&J Pharmtech
AJA-O25643
Academic Data
PubChem
11735918
Names and Identifiers
IUPAC name
4-bromoquinoline
IUPAC Traditional name
4-bromoquinoline
Synonyms
4-Bromoquinoline
4-Bromoquinoline
4-溴喹啉
Registration numbers
PubChem CID
11735918
PubChem SID
162030321
MDL Number
MFCD07644514
CAS Number
3964-04-3
3964/4/3
Properties
Safety Information
MSDS Link
Download link
Source
Download link
Source
Storage Warning
IRRITANT
Source
Irritant/Keep Cold/Light Sensitive/Moisture Sensitive/Store under Argon
Source
TSCA Listed
false
Source
GHS Signal Word
Warning
Source
Safety Statements
26
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
German water hazard class
3
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
Storage Temperature
2-8°C
Source
Product Information
Purity
98%
Source
95%
Source
Empirical Formula (Hill Notation)
C9H6BrN
Source
Physical Property
Flash Point
>110°C
Source
>110 °C
Source
>230 °F
Source
Melting Point
29-34°C
Source
29-34 °C
Source
Molecule Details
Sigma Aldrich
693944
Packaging
1 g in glass bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay