ChemicalBook >> CAS DataBase List >>4-Bromo-1H-indole-7-carboxylic acid

4-Bromo-1H-indole-7-carboxylic acid

CAS No.
1211594-25-0
Chemical Name:
4-Bromo-1H-indole-7-carboxylic acid
Synonyms
4-Bromoindole-7-carboxylic Acid;4-broMo-1H-indole-7-carboxylic acid;1H-Indole-7-carboxylic acid, 4-broMo-
CBNumber:
CB32607064
Molecular Formula:
C9H6BrNO2
Molecular Weight:
240.05
MDL Number:
MFCD12547329
MOL File:
1211594-25-0.mol
Last updated:2025-07-24 18:13:44

4-Bromo-1H-indole-7-carboxylic acid Properties

Boiling point 455.8±30.0 °C(Predicted)
Density 1.838±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka 4.54±0.10(Predicted)
Appearance Light brown to brown Solid
InChI InChI=1S/C9H6BrNO2/c10-7-2-1-6(9(12)13)8-5(7)3-4-11-8/h1-4,11H,(H,12,13)
InChIKey CDTILRQKJWYBOM-UHFFFAOYSA-N
SMILES N1C2=C(C(Br)=CC=C2C(O)=O)C=C1

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H317
Precautionary statements  P280

4-Bromo-1H-indole-7-carboxylic acid price More Price(12)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC B998015 4-Bromo-1H-indole-7-carboxylicAcid 1211594-25-0 10mg $45 2021-12-16 Buy
American Custom Chemicals Corporation HCH0365508 4-BROMO-1H-INDOLE-7-CARBOXYLIC ACID 95.00% 1211594-25-0 5MG $496.64 2021-12-16 Buy
Chemenu CM147931 4-Bromo-1H-indole-7-carboxylicacid 95% 1211594-25-0 1g $500 2021-12-16 Buy
Alichem 1211594250 4-Bromo-1H-indole-7-carboxylicacid 1211594-25-0 1g $525 2021-12-16 Buy
SynChem SC-26955 4-BROMO-1H-INDOLE-7-CARBOXYLIC ACID 95+% 1211594-25-0 1g $750 2021-12-16 Buy
Product number Packaging Price Buy
B998015 10mg $45 Buy
HCH0365508 5MG $496.64 Buy
CM147931 1g $500 Buy
1211594250 1g $525 Buy
SC-26955 1g $750 Buy

4-Bromo-1H-indole-7-carboxylic acid Chemical Properties,Uses,Production

Synthesis

1H-Indole-7-carboxylic acid, 4-broMo-, Methyl ester

1224724-39-3

4-Bromo-1H-indole-7-carboxylic acid

1211594-25-0

To a solution of methyl 4-bromo-1H-indole-7-carboxylate (6 g, 23 mmol, Preparation 1 Step B) in tetrahydrofuran (THF, 300 mL) was added water (60 mL), methanol (MeOH, 60 mL) and lithium hydroxide (2.83 g, 118 mmol). The reaction mixture was heated to reflux and stirred overnight. After completion of the reaction, it was cooled to room temperature and concentrated under reduced pressure to remove the solvent. To the remaining aqueous layer 4N hydrochloric acid (HCl) was slowly added to adjust the pH to about 6. The precipitate precipitated was collected by filtration and the solid was dried to give 4-bromo-1H-indole-7-carboxylic acid (5.5 g, 97% yield). The structure of the product was confirmed by 1H NMR (DMSO-d6): δ 11.39 (br, 1H), 7.65-7.63 (d, J = 8.0 Hz, 1H), 7.46-7.44 (m, 1H), 7.33-7.31 (d, J = 8.0 Hz, 1H), 6.49-6.48 (m, 1H).

References

[1] Patent: WO2014/210255, 2014, A1. Location in patent: Page/Page column 101

4-Bromo-1H-indole-7-carboxylic acid Preparation Products And Raw materials

4-Bromo-1H-indole-7-carboxylic acid Suppliers

Global( 54)Suppliers
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Wuhan TCASChem Technology Co., Ltd. 027-86697669 13986148687 sales@tcaschem.com China 4073 55

4-Bromo-1H-indole-7-carboxylic acid Spectrum

1H-Indole-7-carboxylic acid, 4-broMo- 4-broMo-1H-indole-7-carboxylic acid 4-Bromoindole-7-carboxylic Acid 1211594-25-0