ChemicalBook >> CAS DataBase List >>1H-Indole-3-aceticacid,4-bromo-(9CI)

1H-Indole-3-aceticacid,4-bromo-(9CI)

CAS No.
89245-41-0
Chemical Name:
1H-Indole-3-aceticacid,4-bromo-(9CI)
Synonyms
2-(4-bromo-1H-indol-3-yl)acetic acid;4-Bromoindole-3-acetic Acid;4-Bromo-3-indoleacetic acid;4-broMo-1H-indole-3-acetic acid;1H-Indole-3-acetic acid, 4-broMo-;(4-Bromo-1H-indol-3-yl)-acetic acid;1H-Indole-3-aceticacid,4-bromo-(9CI)
CBNumber:
CB31297828
Molecular Formula:
C10H8BrNO2
Molecular Weight:
254.08
MDL Number:
MFCD09751717
MOL File:
89245-41-0.mol
MSDS File:
SDS
Last updated:2026-05-28 00:57:29

1H-Indole-3-aceticacid,4-bromo-(9CI) Properties

Melting point 185-187℃ (DEC.)
Boiling point 466.0±30.0 °C(Predicted)
Density 1.746
storage temp. 2-8°C
pka 4.27±0.30(Predicted)
Appearance Light yellow to yellow Solid

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

1H-Indole-3-aceticacid,4-bromo-(9CI) price More Price(36)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Matrix Scientific 075814 2-(4-Bromo-1H-indol-3-yl)acetic acid 89245-41-0 1.00g $98 2026-05-18 Buy
Matrix Scientific 075814 2-(4-Bromo-1H-indol-3-yl)acetic acid 89245-41-0 5.00g $333 2026-05-18 Buy
Matrix Scientific 075814 2-(4-Bromo-1H-indol-3-yl)acetic acid 89245-41-0 25.00g $1285 2026-05-18 Buy
aablocks AA0042FY 2-(4-bromo-1H-indol-3-yl)acetic acid 98% 89245-41-0 100mg $32 2026-05-28 Buy
aablocks AA0042FY 2-(4-bromo-1H-indol-3-yl)acetic acid 98% 89245-41-0 250mg $38 2026-05-28 Buy
Product number Packaging Price Buy
075814 1.00g $98 Buy
075814 5.00g $333 Buy
075814 25.00g $1285 Buy
AA0042FY 100mg $32 Buy
AA0042FY 250mg $38 Buy

1H-Indole-3-aceticacid,4-bromo-(9CI) Chemical Properties,Uses,Production

Synthesis

1H-Indole, 1,3-diacetyl-4-bromo-

65018-18-0

1H-Indole-3-aceticacid,4-bromo-(9CI)

89245-41-0

To a dry three-necked flask was added 98.0 kg of 4-bromoindole, 307.0 kg of aluminum trichloride and 500 L of methylene chloride, and 79.0 kg of acetyl chloride was added slowly and dropwise to the three-necked flask. The reaction mixture was heated to 40 °C and kept for 8 hours. Upon completion of the reaction, the mixture was poured into 800 L of ice water, the organic phase was separated and the solvent was recovered to give 1,3-diacetyl-4-bromoindole. Subsequently, 161 kg of morpholine and 40.0 kg of sulfur were added directly to the reaction system, heated to 120 °C and kept for 5 hours. After the rearrangement reaction was completed, 500 L of methanol was added, heated to dissolve, decolorized with activated carbon, filtered and cooled. To the filtrate, 300 L of 70% ethanol and 200 L of 15% sodium hydroxide solution were added and heated to reflux for 4 hours. After completion of the reaction, filter and recover the solvent under vacuum. To the residue, appropriate amount of water was added and the pH was adjusted to 1-2 with dilute hydrochloric acid to precipitate a solid. It was filtered, washed with water to neutral, and finally recrystallized with 60% ethanol to obtain 102.2 kg of 4-bromoindole-3-acetic acid in 85.2% yield.

References

[1] Patent: CN104311469, 2016, B. Location in patent: Paragraph 0070-0072

65018-18-0
89245-41-0
Synthesis of 1H-Indole-3-aceticacid,4-bromo-(9CI) from 1H-Indole, 1,3-diacetyl-4-bromo-
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1H-Indole-3-aceticacid,4-bromo-(9CI) Spectrum

1H-Indole-3-aceticacid,4-bromo-(9CI) 4-broMo-1H-indole-3-acetic acid 4-Bromo-3-indoleacetic acid 1H-Indole-3-acetic acid, 4-broMo- (4-Bromo-1H-indol-3-yl)-acetic acid 4-Bromoindole-3-acetic Acid 2-(4-bromo-1H-indol-3-yl)acetic acid 89245-41-0 INDOLE