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1H-Indole-1-ethanol, 5-broMo-

CAS No.
148366-28-3
Chemical Name:
1H-Indole-1-ethanol, 5-broMo-
Synonyms
5-Bromo-1H-indole-1-ethanol;1H-Indole-1-ethanol, 5-broMo-
CBNumber:
CB52715213
Molecular Formula:
C10H10BrNO
Molecular Weight:
240.1
MDL Number:
MFCD20486677
MOL File:
148366-28-3.mol
MSDS File:
SDS
Last updated:2026-05-28 05:17:14

1H-Indole-1-ethanol, 5-broMo- Properties

storage temp. Sealed in dry,Room Temperature

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P305+P351+P338

1H-Indole-1-ethanol, 5-broMo- price More Price(25)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Matrix Scientific 150622 2-(5-Bromo-1H-indol-1-yl)ethanol 148366-28-3 250.00mg $62 2026-05-18 Buy
Matrix Scientific 150622 2-(5-Bromo-1H-indol-1-yl)ethanol 148366-28-3 1.00g $136 2026-05-18 Buy
Matrix Scientific 150622 2-(5-Bromo-1H-indol-1-yl)ethanol 148366-28-3 5.00g $465 2026-05-18 Buy
Synthonix B52391 2-(5-Bromo-1H-indol-1-yl)ethanol 95+% 148366-28-3 100mg $120 2026-05-06 Buy
Synthonix B52391 2-(5-Bromo-1H-indol-1-yl)ethanol 95+% 148366-28-3 250mg $140 2026-05-06 Buy
Product number Packaging Price Buy
150622 250.00mg $62 Buy
150622 1.00g $136 Buy
150622 5.00g $465 Buy
B52391 100mg $120 Buy
B52391 250mg $140 Buy

1H-Indole-1-ethanol, 5-broMo- Chemical Properties, Uses, Production

Synthesis

ethyl (5-bromo-1H-indol-1-yl)acetate

726174-45-4

1H-Indole-1-ethanol, 5-broMo-

148366-28-3

To a stirred solution of lithium aluminum hydride (LAH, 0.67 g, 3.0 eq.) dissolved in tetrahydrofuran (THF, 10 mL) was slowly added a THF (10 mL) solution of ethyl 2-(5-bromo-1H-indol-1-yl)acetate (Intermediate 28a, 1.7 g, 6.0 mmol) at 0 °C under nitrogen protection. The reaction mixture was continued to be stirred for 2 h at room temperature. Upon completion of the reaction, the reaction was carefully quenched with water and extracted with ethyl acetate. The organic layer was washed sequentially with water and dried over anhydrous sodium sulfate (Na2SO4). The organic layer was concentrated under reduced pressure to give 2-(5-bromo-1H-indol-1-yl)ethanol (0.75 g, yield 51.66%) as a yellow gel.

References

[1] Patent: WO2014/202580, 2014, A1. Location in patent: Page/Page column 95
[2] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 17, p. 2451 - 2454

1H-Indole-1-ethanol, 5-broMo- Preparation Products And Raw materials

Global Suppliers ( 18)
Supplier Tel Email Country ProdList Advantage
Nanjing Norris-Pharm Technology Co., Ltd 13901585132 sales@norris-pharm.com China 8869 55
Shanghai Jian Chao Chemical Technology Co., Ltd. 150-2103-5486 18017383231 983544897@qq.com China 9335 55
Jiangsu Aikon Biopharmaceutical R&D co.,Ltd. 025-66028182 17714375163 yftan@aikonchem.com China 16674 50
Amadis Chemical Company Limited 571-89925085 sales@amadischem.com China 131885 58
Chengdu Saiousi Pharmaceutical Co., Ltd 028-64971018 18108168130 China 1780 55
Zhengzhou Convergence Chemical Co. LTD 13393710386 3941078109@qq.com China 9860 58
Energy Chemical 400-0056266 marketing1@energy-chemical.com China 44927 58
Shanghai Sunway Pharmaceutical Technology Co.,Ltd. 13611835272 13611835272 mmwang@sunwaypharm.com China 44090 58
Bide Pharmatech Ltd. 400-1647117 13681763483 product02@bidepharm.com China 59929 58
Bide Pharmatech Ltd. 400-6005915 sales@picasso-e.com China 39645 58
1H-Indole-1-ethanol, 5-broMo- 5-Bromo-1H-indole-1-ethanol 148366-28-3