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4-Bromo-2-ethylbenzaldehyde

CAS No.
1114808-89-7
Chemical Name:
4-Bromo-2-ethylbenzaldehyde
Synonyms
4-Bromo-2-ethylbenzaldehyde;Benzaldehyde, 4-bromo-2-ethyl-
CBNumber:
CB02464310
Molecular Formula:
C9H9BrO
Molecular Weight:
213.07
MDL Number:
MFCD09835094
MOL File:
1114808-89-7.mol
MSDS File:
SDS
Last updated:2026-09-12 18:48:00

4-Bromo-2-ethylbenzaldehyde Properties

Boiling point 277.7±28.0 °C(Predicted)
Density 1.419±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
Appearance Light yellow to yellow Liquid

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P301+P312-P302+P352-P304+P340-P305+P351+P338

4-Bromo-2-ethylbenzaldehyde price More Price(36)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth PUB80889 4-Bromo-2-ethylbenzaldehyde 1114808-89-7 0.5g $300.9 2026-06-04 Buy
Biosynth PUB80889 4-Bromo-2-ethylbenzaldehyde 1114808-89-7 5g $1180 2026-06-04 Buy
Activate Scientific AS114426 4-Bromo-2-ethylbenzaldehyde 98% 1114808-89-7 1g $223 2026-06-04 Buy
Activate Scientific AS114426 4-Bromo-2-ethylbenzaldehyde 98% 1114808-89-7 5g $752 2026-06-04 Buy
Matrix Scientific 206652 4-Bromo-2-ethylbenzaldehyde 1114808-89-7 250.00mg $67 2026-05-18 Buy
Product number Packaging Price Buy
PUB80889 0.5g $300.9 Buy
PUB80889 5g $1180 Buy
AS114426 1g $223 Buy
AS114426 5g $752 Buy
206652 250.00mg $67 Buy

4-Bromo-2-ethylbenzaldehyde Chemical Properties, Uses, Production

Synthesis

4-BROMO-2-ETHYLIODOBENZENE

175278-30-5

N,N-Dimethylformamide

68-12-2

4-BROMO-2-ETHYLBENZALDEHYDE

1114808-89-7

1. In a dry reaction flask, 4-bromo-2-ethyl-1-iodobenzene (1 equiv.) and anhydrous N,N-dimethylformamide (appropriate amount) are added. 2. Cool the reaction mixture to 0°C under inert gas protection. 3. n-Butyllithium (1.1 eq.) was added slowly, keeping the reaction temperature below 0°C and stirring for 30 minutes. 4. Warm the reaction mixture to room temperature and continue stirring for 2 hours. 5. Monitor the progress of the reaction by thin layer chromatography (TLC) to confirm complete conversion of the feedstock. 6. Upon completion of the reaction, the reaction was quenched by slow addition of dilute hydrochloric acid. 7. Extract the reaction mixture with ethyl acetate and combine the organic phases. 8. 8. The organic phase was dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure. 9. 9. Purify the crude product by column chromatography to obtain 4-bromo-2-ethylbenzaldehyde.

References

[1] Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2016, vol. 55B, # 7, p. 854 - 881
[2] Patent: WO2009/74314, 2009, A1. Location in patent: Page/Page column 170

4-Bromo-2-ethylbenzaldehyde Preparation Products And Raw materials

Global Suppliers ( 40)
Supplier Tel Email Country ProdList Advantage
SynAsst Chemical. 021-60343070 China 12731 55
Hygeia (Chengdu) pharmaceutical technique Co., Ltd 028-84502008 13568869383 sales@hygeiapharm.com China 294 55
Nanjing XiZe Biotechnology CO., Ltd. 025-66023220 15250997978 1511893459@qq.com China 4776 55
BePharm Ltd 400-685-9117 market@bepharm.com China 15081 60
AAB-PHARMA LIMITED 025-66800956 18800000000 sales@njdmchem.com China 4200 50
Amatek Scientific Co. Ltd. 0512-56316828 400-867-5858;400-867-5858 info@amateksci.com China 28759 58
Aikon International Limited 025-58859352 19370895928 sales01@aikonchem.com China 15078 58
Shanghai Jizhi Biochemical Technology Co. Ltd. 021-4009004166/18616739031 18616739031 3007523370@qq.com China 40000 58
Win-Win chemical CO., Limited +86-0086-577-64498589 +86-15355981851 sales@win-winchemical.com China 14297 58
Hefei TNJ Chemical Industry Co.,Ltd. +86-0551-65418684 +86-18949823763 sales@tnjchem.com China 25333 58

4-Bromo-2-ethylbenzaldehyde Spectrum

Benzaldehyde, 4-bromo-2-ethyl- 4-Bromo-2-ethylbenzaldehyde 1114808-89-7