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
SAFETY
Risk and Safety Statements
| Symbol(GHS) | ![]() 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 |
4-Bromo-2-ethylbenzaldehyde Chemical Properties, Uses, Production
Synthesis
175278-30-5
68-12-2
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
Raw materials
Preparation Products
| Supplier | Tel | 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 |
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