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Molecule
ID:10097
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₆BrN
Molecular Mass
196.04394
Exact Mass
194.9683612
Charge
0
InChI
InChI=1S/C8H6BrN/c9-7-2-1-3-8-6(7)4-5-10-8/h1-5,10H
InChIKey
GRJZJFUBQYULKL-UHFFFAOYSA-N
Canonic Smiles
Brc1cccc2c1cc[nH]2
Isomeric Smiles
c1ccc2c(c1Br)cc[nH]2
Calculated Properties
JChem
Acid pKa
16.143888
H Acceptors
0
H Donor
1
LogD (pH = 5.5)
2.8407605
LogD (pH = 7.4)
2.8407605
Log P
2.8407605
Molar Refractivity
44.7673
Polarizability
18.209932
Polar Surface Area
15.79
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
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RDKit
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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
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IUPAC name
Registration numbers
Properties
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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
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TRC
References
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PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR5639
Maybridge
RH01101
Matrix Scientific
006845
Sigma Aldrich
524336
TRC
B684480
Alfa Aesar
L19417
Chemik
CHH14700
Enamine
EN300-102700
Bide Pharmatech
BD5840
A&J Pharmtech
AJA-O5758
AJA-O40008
Academic Data
PubChem
676494
Names and Identifiers
Synonyms
4-Bromoindole
4-Bromo-1H-indole
4-Bromoindole
4-溴吲哚
4-Bromo-1H-indole
IUPAC Traditional name
4-bromo-1H-indole
IUPAC name
4-bromo-1H-indole
Registration numbers
CAS Number
52488-36-5
19053-14-6
MDL Number
MFCD00671502
PubChem SID
24874403
160973404
PubChem CID
676494
EC Number
000-000-0
Beilstein Number
114891
Molecule Details
Sigma Aldrich
524336
Packaging
1, 5 mL in glass bottle
TRC
B684480
A potential inhibitor of GSK-3.
References
PubChem Literature
From Data Sources
•
Meijer, L., et al.: Chem. Biol., 10, 1255 (2001)
•
Leclerc, S., et al.: J. Biol. Chem., 276, 251 (2001)
•
Noble, M., et al.: Science, 303, 1800 (2001)
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
MDL Number
•
PubChem SID
•
PubChem CID
•
EC Number
•
Beilstein Number
Properties
Safety Information
Storage Warning
IRRITANT, KEEP COLD
Source
Harmful/Light Sensitive/Keep Cold/Store under Argon
Source
Air & Light Sensitive
Source
MSDS Link
Download link
Source
Download link
Source
Download link
Source
TSCA Listed
false
Source
否
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
Safety Statements
26
-
36
Source
Risk Statements
36/37/38
Source
GHS Signal Word
Warning
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
German water hazard class
3
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
European Hazard Symbols
Irritant (Xi)
Source
Storage Condition
Refrigerator
Source
Physical Property
Melting Point
17°C
Source
17°C
Source
Refractive Index
1.6550
Source
1.655
Source
n20/D 1.655(lit.)
Source
1.6545
Source
Boiling Point
88-90°C/0.1mm
Source
283-285 °C(lit.)
Source
88-90°C/0.1mm
Source
1.563
Source
1.563 g/mL at 25 °C(lit.)
Source
>110°C
Source
110 °C
Source
230 °F
Source
>110°C(230°F)
Source
Ethyl Acetate
Source
Chloroform
Source
Yellow Oil
Source
3.163
Source
Product Information
Purity
95%
Source
97%
Source
96%
Source
98%
Source
Empirical Formula (Hill Notation)
C8H6BrN
Source
Certificate of Analysis
Download link
Source
Density
Flash Point
Solubility
Apperance
Hydrophobicity(logP)