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ChemicalBook >> CAS DataBase List >>5-BROMO-1-ETHYL-1H-INDOLE

5-BROMO-1-ETHYL-1H-INDOLE

CAS No.
195253-49-7
Chemical Name:
5-BROMO-1-ETHYL-1H-INDOLE
Synonyms
5-bromo-1-ethylindole;5-BROMO-1-ETHYL-1H-INDOLE;1-ethyl-5-bromo-1H-indole;1H-Indole, 5-bromo-1-ethyl-;5-Bromo-1-ethyl-1H-indole , 5-Bromo-1-ethyl-1H-indole
CBNumber:
CB82463995
Molecular Formula:
C10H10BrN
Molecular Weight:
224.1
MDL Number:
MFCD04344211
MOL File:
195253-49-7.mol
MSDS File:
SDS
Last updated:2026-05-28 03:45:06
Product description Number Pack Size Price
5-Bromo-1-ethyl-1H-indole 97% AS48557 1g $47
5-Bromo-1-ethyl-1H-indole 97% AS48557 5g $135
5-Bromo-1-ethyl-1H-indole 97% AS48557 25g $432
5-Bromo-1-ethyl-1H-indole 97% B52351 1g $87
5-Bromo-1-ethyl-1H-indole 97% B52351 5g $100

5-BROMO-1-ETHYL-1H-INDOLE Properties

storage temp. Sealed in dry,Room Temperature
Appearance Colorless to light 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-P305+P351+P338

5-BROMO-1-ETHYL-1H-INDOLE price More Price(23)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Activate Scientific AS48557 5-Bromo-1-ethyl-1H-indole 97% 195253-49-7 1g $47 2026-06-04 Buy
Activate Scientific AS48557 5-Bromo-1-ethyl-1H-indole 97% 195253-49-7 5g $135 2026-06-04 Buy
Activate Scientific AS48557 5-Bromo-1-ethyl-1H-indole 97% 195253-49-7 25g $432 2026-06-04 Buy
Synthonix B52351 5-Bromo-1-ethyl-1H-indole 97% 195253-49-7 1g $87 2026-05-06 Buy
Synthonix B52351 5-Bromo-1-ethyl-1H-indole 97% 195253-49-7 5g $100 2026-05-06 Buy
Product number Packaging Price Buy
AS48557 1g $47 Buy
AS48557 5g $135 Buy
AS48557 25g $432 Buy
B52351 1g $87 Buy
B52351 5g $100 Buy

5-BROMO-1-ETHYL-1H-INDOLE Chemical Properties,Uses,Production

Synthesis

5-Bromoindole

10075-50-0

Iodoethane

75-03-6

5-BROMO-1-ETHYL-1H-INDOLE

195253-49-7

Example 15 General procedure for the synthesis of 5-bromo-3-(2,4-dichlorobenzoyl)-1-ethyl-1H-indole: 1a) Synthesis of 5-bromo-1-ethyl-1H-indole In 75 mL of anhydrous dimethylformamide (DMF), 3.06 g (76.5 mmol, 60% mineral oil suspension) of sodium hydride (NaH) was added. The mixture was stirred and heated to 80 °C. Subsequently, 5.0 g (25.5 mmol) of 5-bromo-1H-indole was slowly added. The heating was continued for 30 minutes (until the hydrogen gas stopped being released). The reaction mixture was cooled to room temperature and 4 mL (51 mmol) of ethyl iodide was added. The mixture was again heated to 80 °C and the reaction was maintained for 2 hours. Upon completion of the reaction, hydrolysis was carried out. The reaction mixture was extracted with dichloromethane and the organic phase was dried with anhydrous sodium sulfate and concentrated. The concentrated residue was purified by silica gel column chromatography using dichloromethane as eluent to give the target product (Int.49). Yield: 89% as a yellow oil.

References

[1] Archiv der Pharmazie, 1997, vol. 330, # 5, p. 141 - 145
[2] Patent: US2004/67998, 2004, A1. Location in patent: Page/Page column 18

5-BROMO-1-ETHYL-1H-INDOLE Preparation Products And Raw materials

5-BROMO-1-ETHYL-1H-INDOLE Suppliers

Global( 47)Suppliers
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5-BROMO-1-ETHYL-1H-INDOLE Spectrum

5-BROMO-1-ETHYL-1H-INDOLE 5-Bromo-1-ethyl-1H-indole , 5-Bromo-1-ethyl-1H-indole 1-ethyl-5-bromo-1H-indole 1H-Indole, 5-bromo-1-ethyl- 5-bromo-1-ethylindole 195253-49-7
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