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  8. 2-Bromo-5-fluorobenzaldehyde, 98%, Thermo Scientific Chemicals

2-Bromo-5-fluorobenzaldehyde, 98%, Thermo Scientific Chemicals

Catalog Number AAB2507114
Click to view available options
Quantity:
5 g
25 g
94569-84-3
C7H4BrFO
203.01
MFCD00142872
CJUCIKJLMFVWIS-UHFFFAOYSA-N
benzaldehyde, 2-bromo-5-fluoro, 2-bromo-5-fluorobenzaldhyde, 5-fluoro-2-bromo benzaldehyde, 2-bromo-5-fluoro-benzaldehyde, pubchem1418, acmc-209rsk, ksc494g0d, 2-bromo-5-fluoro benzaldehyde, 2-bromo-5-fluorobenzaldehyde
2773321
2-bromo-5-fluorobenzaldehyde
C1=CC(=C(C=C1F)C=O)Br
94569-84-3
C7H4BrFO
203.01
MFCD00142872
CJUCIKJLMFVWIS-UHFFFAOYSA-N
benzaldehyde, 2-bromo-5-fluoro, 2-bromo-5-fluorobenzaldhyde, 5-fluoro-2-bromo benzaldehyde, 2-bromo-5-fluoro-benzaldehyde, pubchem1418, acmc-209rsk, ksc494g0d, 2-bromo-5-fluoro benzaldehyde, 2-bromo-5-fluorobenzaldehyde
2773321
2-bromo-5-fluorobenzaldehyde
C1=CC(=C(C=C1F)C=O)Br

Description

2-Bromo-5-fluorobenzaldehyde is used as a precursor for the synthesis of 5-fluoro-3-substituted benzoxaboroles, which is used in material science as molecular receptors, building block in crystal engineering, as steroid conjugates for molecular imprinting , dyes and biosensors of alpha hydroxyl carboxylic acids. It is also used in the synthesis of 5-arylindazolo[3,2-b]quinazolin-7(5H)-one by reacting with 2-amino-N'-arylbenzohydrazide in the presence of Copper(I) bromide by the Ullmann-type reaction.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
2-Bromo-5-fluorobenzaldehyde is used as a precursor for the synthesis of 5-fluoro-3-substituted benzoxaboroles, which is used in material science as molecular receptors, building block in crystal engineering, as steroid conjugates for molecular imprinting , dyes and biosensors of alpha hydroxyl carboxylic acids. It is also used in the synthesis of 5-arylindazolo[3,2-b]quinazolin-7(5H)-one by reacting with 2-amino-N′-arylbenzohydrazide in the presence of Copper(I) bromide by the Ullmann-type reaction.

Solubility
Soluble in methanol.

Notes
Air sensitive. Keep container tightly closed in a cool, dry and well-ventilated place.
TRUSTED_SUSTAINABILITY
Melting Point 51°C to 56°C
Flash Point 87°C (190°F)
Quantity 25 g
Sensitivity Air Sensitive
Solubility Information Soluble in methanol.
Formula Weight 203.01
Percent Purity 98%
Chemical Name or Material 2-Bromo-5-fluorobenzaldehyde

Safety and Handling

Hazard Category H302+H312+H332-H315-H319-H335-H500
Hazard Statement GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
Precautionary Statement P261-P264b-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P362-P501c
TSCA No
Recommended Storage Ambient temperatures
SDS

RUO – Research Use Only

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