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Molecule
ID:6896
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₄BrFO
Molecular Mass
203.0084632
Exact Mass
201.94295497
Charge
0
InChI
InChI=1S/C7H4BrFO/c8-6-1-2-7(9)5(3-6)4-10/h1-4H
InChIKey
MMFGGDVQLQQQRX-UHFFFAOYSA-N
Canonic Smiles
O=Cc1cc(Br)ccc1F
Isomeric Smiles
O=Cc1c(ccc(c1)Br)F
Calculated Properties
JChem
H Acceptors
1
H Donor
0
LogD (pH = 5.5)
2.5972028
LogD (pH = 7.4)
2.5972028
Log P
2.5972028
Molar Refractivity
40.4812
Polarizability
14.921654
Polar Surface Area
17.07
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
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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
•
Synonyms
•
IUPAC Traditional name
Registration numbers
Properties
•
Safety Information
•
Physical Property
•
Product Information
Related Proteins
Molecular Spectra
Molecule Details
•
Apollo Scientific
•
Sigma Aldrich
•
TRC
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
PC1399G
Matrix Scientific
001723
InterBioScreen
BB_SC-4541
Sigma Aldrich
528870
TRC
B684525
Chemik
CHB20200
Bide Pharmatech
BD10251
Alfa Aesar
A14219
Academic Data
PubChem
736327
Names and Identifiers
IUPAC name
5-bromo-2-fluorobenzaldehyde
Synonyms
5-Bromo-2-fluorobenzaldehyde
5-Bromo-2-fluorobenzaldehyde 98%
2-Fluoro-5-bromobenzaldehyde
5-Bromo-2-fluorobenzaldehyde
5-溴-2-氟苯甲醛
2-Fluoro-5-bromobenzaldehyde
3-Bromo-6-fluorobenzaldehyde
IUPAC Traditional name
5-bromo-2-fluorobenzaldehyde
Registration numbers
EC Number
298-056-6
CAS Number
93777-26-5
Beilstein Number
7632798
MDL Number
MFCD00070755
PubChem SID
24877622
160970203
PubChem CID
736327
Molecule Details
Apollo Scientific
PC1399G
Store at 2-8°C
Sigma Aldrich
528870
Packaging
25 g in glass bottle
TRC
B684525
5-Bromo-2-fluorobenzaldehyde is used for the preparation of benzimidazole derivatives as inhibitors of leukotriene production.
References
PubChem Literature
From Data Sources
•
Werz, et al.: Expert. Opin. Ther. Patents, 15, 505 (2005)
Bioactivity
PubChem BioAssay
Registration numbers
•
EC Number
•
CAS Number
•
Beilstein Number
•
MDL Number
•
PubChem SID
•
PubChem CID
Properties
Safety Information
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Storage Warning
IRRITANT
Source
Irritant/Light Sensitive/Air Sensitive/Store under Argon/Keep Cold
Source
Air Sensitive
Source
TSCA Listed
false
Source
否
Source
Storage Condition
Store at 2-8°C
Source
Personal Protective Equipment
Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
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
GHS Signal Word
Warning
Source
European Hazard Symbols
Irritant (Xi)
Source
German water hazard class
3
Source
Safety Statements
26
-
36
Source
26
-
37
Source
Risk Statements
36/37/38
Source
Storage Temperature
2-8°C
Source
Physical Property
Density
1.710
Source
1.71
Source
1.71 g/mL at 25 °C(lit.)
Source
Refractive Index
1.5700
Source
1.57
Source
n20/D 1.57(lit.)
Source
Melting Point
23°C
Source
109°C
Source
228.2 °F
Source
109 °C
Source
109°C(228°F)
Source
230°C
Source
230 °C(lit.)
Source
230°C
Source
Product Information
Purity
98%
Source
97%
Source
Linear Formula
BrC6H3(F)CHO
Source
Certificate of Analysis
Download link
Source
Flash Point
Boiling Point