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Molecule
ID:70628
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₄Br₂O
Molecular Mass
263.91406
Exact Mass
261.86288875
Charge
0
InChI
InChI=1S/C7H4Br2O/c8-6-1-5(4-10)2-7(9)3-6/h1-4H
InChIKey
ZLDMZIXUGCGKMB-UHFFFAOYSA-N
Canonic Smiles
O=Cc1cc(Br)cc(c1)Br
Isomeric Smiles
C(=O)c1cc(cc(c1)Br)Br
Calculated Properties
JChem
H Acceptors
1
H Donor
0
LogD (pH = 5.5)
3.2232535
LogD (pH = 7.4)
3.2232535
Log P
3.2232535
Molar Refractivity
47.8876
Polarizability
18.15252
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
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
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RDKit
•
JChem
Data Source
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Academic Data
Names and Identifiers
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IUPAC Traditional name
•
IUPAC name
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Synonyms
Registration numbers
Properties
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Product Information
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Safety Information
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Physical Property
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
•
PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
076196
Apollo Scientific
OR4526
Sigma Aldrich
515396
Bide Pharmatech
BD4112
Alfa Aesar
B25495
Academic Data
PubChem
622077
Names and Identifiers
IUPAC Traditional name
3,5-dibromobenzaldehyde
IUPAC name
3,5-dibromobenzaldehyde
Synonyms
3,5-Dibromobenzaldehyde
3,5-二溴苯甲醛
3,5-Dibromobenzaldehyde
Registration numbers
MDL Number
MFCD00156887
CAS Number
56990-02-4
PubChem SID
162036343
24873818
PubChem CID
622077
Beilstein Number
2573432
EC Number
000-000-0
Molecule Details
Sigma Aldrich
515396
Packaging
5 g in glass bottle
Application
Reactant involved in:
• Suzuki-Miyaura cross-coupling reactions1
• Synthesis of blue fluorescent dye derivatives for organic light emitting diodes2
• Sharpless kinetic resolution for the formation of Baylis-Hillman enal adducts3
• Synthesis of podophyllotoxin mimetic pyridopyrazoles as anticancer agents4
• Allylic alkylation5
• Synthesis of C2-symmetric biphosphine ligand I6
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
MDL Number
•
CAS Number
•
PubChem SID
•
PubChem CID
•
Beilstein Number
•
EC Number
Properties
Product Information
Purity
95+%
Source
98%
Source
Linear Formula
Br2C6H3CHO
Source
Safety Information
TSCA Listed
false
Source
否
Source
Storage Warning
IRRITANT
Source
Corrosive/Light Sensitive/Air Sensitive/Store under Argon
Source
Air Sensitive
Source
Download link
Source
Download link
Source
H314
Source
H315
-
H319
-
H335
Source
3261
Source
Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
Source
Danger
Source
P280
-
P305+P351+P338
-
P310
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
UN 3261 8/PG 2
Source
8
Source
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
Corrosive (C)
26
-
36/37/39
-
45
Source
26
-
37
Source
3
Source
34
Source
36/37/38
Source
2
Source
Physical Property
89.7-91.5°C
Source
84-88 °C(lit.)
Source
89-93°C
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
MSDS Link
GHS Hazard statements
UN Number
Personal Protective Equipment
GHS Signal Word
GHS Precautionary statements
RID/ADR
Hazard Class
GHS Pictograms
European Hazard Symbols
Safety Statements
German water hazard class
Risk Statements
Packing Group
Melting Point