Substance
ID:335426
Names and Identifiers
IUPAC name
4-bromobenzaldehyde
IUPAC Traditional name
benzaldehyde, 4-bromo-
Synonyms
4-Bromobenzaldehyde4-溴苯甲醛
Registration numbers
EC Number
MDL Number
Beilstein Number
CAS Number
PubChem SID
Properties
Product Information
Grade
ReagentPlus®
Linear Formula
BrC6H4CHO
Purity
99%
Safety Information
GHS Signal Word
Danger
European Hazard Symbols
Harmful (Xn)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
Respiratory sensitization, category 1
Germ cell mutagenicity, categories 1A,1B,2
Carcinogenicity, categories 1A,1B,2
Reproductive toxicity, categories 1A,1B,2
Specific Target Organ Toxicity – Single exposure, categories 1,2
Specific Target Organ Toxicity – Repeated exposure, categories 1,2
Aspiration Hazard, category 1
GHS Hazard statements
H302-H315-H319-H334-H335
MSDS Link
GHS Precautionary statements
P261-P305+P351+P338-P342+P311
RTECS
CU4810000
Safety Statements
26-36/37
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Risk Statements
22-36/37/38-43
German water hazard class
2
Physical Property
Melting Point
55-58 °C(lit.)
Flash Point
228.2 °F
109 °C
Molecule Details
Application
Employed in palladium-catalyzed mono- and bis-arylation of 3,4-(ethylenedioxy)thiophenes.1 Also used in a cross-coupling study with potassium vinyltrifluoroborate.2
Packaging
10, 25, 100 g in glass bottle
Legal Information
ReagentPlus is a registered trademark of Sigma-Aldrich Co. LLC
Employed in palladium-catalyzed mono- and bis-arylation of 3,4-(ethylenedioxy)thiophenes.1 Also used in a cross-coupling study with potassium vinyltrifluoroborate.2
Packaging
10, 25, 100 g in glass bottle
Legal Information
ReagentPlus is a registered trademark of Sigma-Aldrich Co. LLC
Molecular Spectra
No Data Available
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References
No Data Available
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