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Molecule
ID:13766
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₅H₃BrIN
Molecular Mass
283.89249
Exact Mass
282.8493591
Charge
0
InChI
InChI=1S/C5H3BrIN/c6-4-1-2-5(7)8-3-4/h1-3H
InChIKey
HSNBRDZXJMPDGH-UHFFFAOYSA-N
Canonic Smiles
Ic1ccc(cn1)Br
Isomeric Smiles
c1(cnc(cc1)I)Br
Calculated Properties
JChem
H Acceptors
1
H Donor
0
LogD (pH = 5.5)
2.485857
LogD (pH = 7.4)
2.4858582
Log P
2.4858582
Molar Refractivity
44.5945
Polarizability
17.893974
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
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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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Names and Identifiers
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Synonyms
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IUPAC Traditional name
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IUPAC name
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Properties
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Physical Property
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Product Information
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR1964
Matrix Scientific
011251
ChemBridge
4045186
Sigma Aldrich
569607
Chemik
CHH00611
Enamine
EN300-105367
Bide Pharmatech
BD8359
Alfa Aesar
L19610
A&J Pharmtech
AJA-O40062
Academic Data
PubChem
593690
Names and Identifiers
Synonyms
5-Bromo-2-iodopyridine
5-溴-2-碘吡啶
5-Bromo-2-iodopyridine
IUPAC Traditional name
5-bromo-2-iodopyridine
IUPAC name
5-bromo-2-iodopyridine
Registration numbers
CAS Number
223463-13-6
PubChem CID
593690
MDL Number
MFCD00691506
PubChem SID
160977073
24880511
Beilstein Number
2119
EC Number
000-000-0
Properties
Physical Property
Melting Point
113-114°C
Source
113-117°C
Source
113-117 °C(lit.)
Source
113 - 117°C
Source
113-116°C
Source
Hydrophobicity(logP)
2.444
Source
Safety Information
Storage Warning
IRRITANT, LIGHT SENSITIVE
Source
Irritant/Light Sensitive/Store under Argon/Keep Cold
Source
Light Sensitive
Source
TSCA Listed
false
Source
否
Source
MSDS Link
Download link
Source
Download link
Source
Safety Statements
26
-
36
Source
26
-
37
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
GHS Hazard statements
H315
-
H319
-
H335
Source
European Hazard Symbols
Irritant (Xi)
Source
Risk Statements
36/37/38
Source
GHS Signal Word
Warning
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
Product Information
Purity
98%
Source
97%
Source
95%
Source
Empirical Formula (Hill Notation)
C5H3BrIN
Source
Molecule Details
Sigma Aldrich
569607
Packaging
5, 25 g in glass bottle
References
PubChem Literature
From Data Sources
•
Conditions have been described for the generation of 5-bromo-2-pyridylmagnesium chloride, using isopropylmagnesium chloride, and its subsequent reaction with electrophiles to give various 2-substituted 5-bromopyridines:
Org. Lett.
,
6
, 4905 (2004).
Bioactivity
PubChem BioAssay
Registration numbers
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CAS Number
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PubChem CID
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MDL Number
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PubChem SID
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Beilstein Number
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EC Number