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Molecule
ID:6640
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₃BrF₃N
Molecular Mass
225.9939296
Exact Mass
224.94009576
Charge
0
InChI
InChI=1S/C6H3BrF3N/c7-5-2-1-4(3-11-5)6(8,9)10/h1-3H
InChIKey
GSKMWMFOQQBVMI-UHFFFAOYSA-N
Canonic Smiles
Brc1ccc(cn1)C(F)(F)F
Isomeric Smiles
c1(cnc(cc1)Br)C(F)(F)F
Calculated Properties
JChem
H Acceptors
1
H Donor
0
LogD (pH = 5.5)
2.6076932
LogD (pH = 7.4)
2.6076965
Log P
2.6076965
Molar Refractivity
38.3398
Polarizability
13.983535
Polar Surface Area
12.89
Rotatable Bonds
1
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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IUPAC name
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IUPAC Traditional name
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PubChem CID
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MDL Number
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PubChem SID
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Product Information
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Molecular Spectra
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Sigma Aldrich
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
001382
Apollo Scientific
PC1598G
Maybridge
SPB05624
Sigma Aldrich
661120
Chemik
CHH00209
Bide Pharmatech
BD3117
Alfa Aesar
43381
A&J Pharmtech
AJA-O4335
AJA-O12333
Academic Data
PubChem
2736434
Names and Identifiers
Synonyms
2-Bromo-5-(trifluoromethyl)pyridine
2-Bromo-5-(trifluoromethyl)pyridine 97%
2-Bromo-5-(trifluoromethyl)pyridine
2-溴-5-(三氟甲基)吡啶
IUPAC name
2-bromo-5-(trifluoromethyl)pyridine
IUPAC Traditional name
2-bromo-5-(trifluoromethyl)pyridine
Registration numbers
CAS Number
50488-42-1
PubChem CID
2736434
MDL Number
MFCD00153086
PubChem SID
160969947
24884504
Molecule Details
Sigma Aldrich
661120
Application
Substrate used in a palladium-catalyzed α-arylation of a Refomatsky reagent.1
Packaging
1, 5 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Physical Property
Melting Point
45-47°C
Source
44-48°C
Source
44-48 °C
Source
45-47°C
Source
Boiling Point
78-81°C/30mm
Source
78-81°C/30mm
Source
Apperance
Crystalline
Source
Safety Information
Storage Warning
IRRITANT
Source
Toxic
Source
TSCA Listed
false
Source
否
Source
MSDS Link
Download link
Source
Download link
Source
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
25
-
36/37/38
Source
36/37/38
Source
Danger
Source
Toxic (T)
H300
-
H315
-
H319
-
H335
Source
H315
-
H319
-
H335
Source
6.1
Source
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Source
UN 2811 6.1/PG 3
Source
2811
Source
P261
-
P264
-
P301+P310
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
3
Source
3
Source
26
-
37
Source
Product Information
Purity
97%
Source
95%
Source
96%
Source
98%
Source
Empirical Formula (Hill Notation)
C6H3BrF3N
Source
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
Source
Source
Irritant (Xi)
Source
Source
GHS Pictograms
Risk Statements
GHS Signal Word
European Hazard Symbols
GHS Hazard statements
Hazard Class
Personal Protective Equipment
RID/ADR
UN Number
GHS Precautionary statements
German water hazard class
Packing Group
Safety Statements