ChemicalBook >> CAS DataBase List >>6-BROMO-5-FLUOROINDOLIN-2-ONE

6-BROMO-5-FLUOROINDOLIN-2-ONE

CAS No.
893620-44-5
Chemical Name:
6-BROMO-5-FLUOROINDOLIN-2-ONE
Synonyms
6-Bromo-5-fluoro-2-indolinone;6-BROMO-5-FLUOROINDOLIN-2-ONE;6-Bromo-5-fluoro-1,3-dihydro-2H-indol-2-one;2H-Indol-2-one, 6-bromo-5-fluoro-1,3-dihydro-
CBNumber:
CB42665292
Molecular Formula:
C8H5BrFNO
Molecular Weight:
230.03
MDL Number:
MFCD16250437
MOL File:
893620-44-5.mol
MSDS File:
SDS
Last updated:2026-05-28 04:35:28
Product description Number Pack Size Price
6-Bromo-5-fluoroindolin-2-one 95% PC201365 100mg $39
6-Bromo-5-fluoroindolin-2-one 95% PC201365 250mg $81
6-Bromo-5-fluoroindolin-2-one 95% PC201365 1g $263
6-Bromo-5-fluoroindolin-2-one 95% PC201365 5g $1072
6-Bromo-5-fluoroindolin-2-one 95% PC201365 100mg $39

6-BROMO-5-FLUOROINDOLIN-2-ONE Properties

Boiling point 334.4±42.0 °C(Predicted)
Density 1.749±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka 12.04±0.20(Predicted)
Appearance Light brown to yellow Solid

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H317-H319
Precautionary statements  P280-P305+P351+P338
HS Code  2933998090

6-BROMO-5-FLUOROINDOLIN-2-ONE price More Price(54)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Apolloscientific PC201365 6-Bromo-5-fluoroindolin-2-one 95% 893620-44-5 100mg $39 2026-06-04 Buy
Apolloscientific PC201365 6-Bromo-5-fluoroindolin-2-one 95% 893620-44-5 250mg $81 2026-06-04 Buy
Apolloscientific PC201365 6-Bromo-5-fluoroindolin-2-one 95% 893620-44-5 1g $263 2026-06-04 Buy
Apolloscientific PC201365 6-Bromo-5-fluoroindolin-2-one 95% 893620-44-5 5g $1072 2026-06-04 Buy
Apolloscientific PC201365 6-Bromo-5-fluoroindolin-2-one 95% 893620-44-5 100mg $39 2026-06-04 Buy
Product number Packaging Price Buy
PC201365 100mg $39 Buy
PC201365 250mg $81 Buy
PC201365 1g $263 Buy
PC201365 5g $1072 Buy
PC201365 100mg $39 Buy

6-BROMO-5-FLUOROINDOLIN-2-ONE Chemical Properties,Uses,Production

Synthesis

1-BROMO-2,4-DIFLUORO-5-NITROBENZENE

345-24-4

Dimethyl malonate

108-59-8

6-BROMO-5-FLUOROINDOLIN-2-ONE

893620-44-5

a) Synthesis of dimethyl 2-(4-bromo-5-fluoro-2-nitrophenyl)-malonate/2-(2-bromo-5-fluoro-4-nitrophenyl)-dimethyl malonate mixture A: Suspension of NaH (60% dispersed in mineral oil, 20.2 g, 504 mmol) in dioxane (233 ml) and cooling to 11 °C. A solution of 1-bromo-2,4-difluoro-5-nitrobenzene (50 g, 26.5 ml, 210 mmol) and dimethyl malonate (33.3 g, 28.9 ml, 242 mmol) in dioxane (467 ml) was slowly added at 11 °C. The temperature was raised to 14°C in 45 min (note the gas release). After addition, the reaction mixture was kept at 12 °C for 1 h and then raised to room temperature.After 16 h, the reaction mixture was cooled to 10 °C and 100 ml of saturated aqueous ammonium chloride solution was added. The reaction mixture was diluted with tert-butyl methyl ether, water and saturated aqueous ammonium chloride solution. The aqueous phase was extracted with tert-butyl methyl ether and the combined organic phases were washed with saturated aqueous ammonium chloride solution and brine and dried over sodium sulfate. The solvent was evaporated and the residue was purified by silica gel chromatography using ethyl acetate/heptane as eluent. 6-Bromo-5-fluoroindolin-2-one was obtained as a yellow liquid (53.7 g) as a 2.6:1 mixture and was used directly in the next reaction. b) Hydrolysis reaction: Dimethyl 2-(4-bromo-5-fluoro-2-nitrophenyl)-propanedioate/2-(2-bromo-5-fluoro-4-nitrophenyl)-propanedioic acid dimethyl ester (2.6:1 mixture, 53.7 g, 153 mmol) was heated and refluxed with 6 M aqueous hydrochloric acid (767 ml) for 7 h. It was cooled down to 5 °C. The precipitate was precipitated with water and n-pentylamine. The precipitate was filtered, washed with water and n-pentane, then co-evaporated with toluene three times to give 25.9 g of 6-bromo-5-fluoroindolin-2-one as a white solid. The mother liquor was extracted with ethyl acetate and the combined organic phases were dried over sodium sulfate. The solvent was evaporated and the residue was ground with n-pentane and then co-evaporated with toluene to give 11.42 g of 6-bromo-5-fluoroindolin-2-one as an off-white solid. The two batches were combined to give a total of 37.32 g of 6-bromo-5-fluoroindolin-2-one as a 2.6:1 mixture, which was used directly in the next step of the reaction. c) Reduction reaction: A solution (671 ml) of (4-bromo-5-fluoro-2-nitrophenyl)-acetic acid/(2-bromo-5-fluoro-4-nitrophenyl)-acetic acid (2.6:1 mixture, 37.3 g, 134 mmol) and iron powder (30.0 g, 537 mmol) in acetic acid was heated and kept at 100 °C for 7 h. The solution was cooled to room temperature. The remaining iron powder was removed with a magnet. Ice water (900 ml) was added to the reaction mixture. The precipitate was filtered, washed four times with water and then suspended in cold water with 25% HCl (300 ml) and concentrated hydrochloric acid (50 ml).After 10 min, the precipitate was filtered and washed four times with water. The precipitate was suspended in a mixture of 1 M Na2CO3 aqueous solution (400 ml) and 0.1 M NaOH (100 ml) and stirred for 40 min. The precipitate was filtered and washed four times with 0.1 M NaOH aqueous solution, three times with water and once with diisopropyl ether to give 6-bromo-5-fluoroindolin-2-one (20.5 g) as a light gray solid.MS ESI (m/z): 228.0/230.0 [(M+H)+].1H NMR (DMSO-D6, 400MHz): δ (ppm) = 10.47 (bs, 1H), 7.31-7.28 (m, 1H), 7.01-6.99 (m, 1H), 3.49 (s, 2H).

References

[1] Patent: WO2014/40969, 2014, A1. Location in patent: Page/Page column 29-30
[2] Patent: WO2014/202493, 2014, A1. Location in patent: Page/Page column 54; 55

345-24-4
108-59-8
893620-44-5
Synthesis of 6-BROMO-5-FLUOROINDOLIN-2-ONE from 1-BROMO-2,4-DIFLUORO-5-NITROBENZENE and Dimethyl malonate

6-BROMO-5-FLUOROINDOLIN-2-ONE Preparation Products And Raw materials

6-BROMO-5-FLUOROINDOLIN-2-ONE Suppliers

Global( 69)Suppliers
Supplier Tel Email Country ProdList Advantage
career henan chemical co
+86-0371-86658258 +8613203830695 factory@coreychem.com China 29792 58
Guangzhou Yuheng Pharmaceutical Technology Co., Ltd
+8613580539051 joe@yuhengpharm.com CHINA 21142 58
Hubei Ipure Biology Co., Ltd
+8613367258412 ada@ipurechemical.com China 10236 58
Finetech Industry Limited
+86-27-8746-5837 +8619945049750 info@finetechnology-ind.com China 9539 58
SUZHOU SENFEIDA CHEMICAL CO.,LTD
+86-0512-83500002 +8618662433356 3899766280@qq.com China 26362 58
HANGZHOU LEAP CHEM CO., LTD.
+86-571-87711850 market18@leapchem.com China 43333 58
Aladdin Scientific
tp@aladdinsci.com United States 52923 58
NANJING YINGWEN BIOTECHNOLOGY CO LTD
+8613382787392 sales@aeechem.com China 10001 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131957 58
Changzhou Huanling Chemical Co., Ltd. 89803005 18206112582 info@huanlingchem.com China 983 68

View Lastest Price from 6-BROMO-5-FLUOROINDOLIN-2-ONE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
6-BROMO-5-FLUOROINDOLIN-2-ONE pictures 2020-01-13 6-BROMO-5-FLUOROINDOLIN-2-ONE
893620-44-5
$9.80 1g ≥99% 100kg Career Henan Chemical Co

6-BROMO-5-FLUOROINDOLIN-2-ONE Spectrum

6-BROMO-5-FLUOROINDOLIN-2-ONE 2H-Indol-2-one, 6-bromo-5-fluoro-1,3-dihydro- 6-Bromo-5-fluoro-2-indolinone 6-Bromo-5-fluoro-1,3-dihydro-2H-indol-2-one 893620-44-5