ChemicalBook >> CAS DataBase List >>3-ACETOXY-5-BROMOINDOLE
3-ACETOXY-5-BROMOINDOLE
- CAS No.
- 17357-14-1
- Chemical Name:
- 3-ACETOXY-5-BROMOINDOLE
- Synonyms
- 5-BROMOINDOXYL ACETATE;5-BROMOINDOLYL ACETATE;O-ACETYL-5-BROMOINDOXYL;3-ACETOXY-5-BROMOINDOLE;5-BROMOINDOXYL-3-ACETATE;5-BROMOINDOLYL 3-ACETATE;5-Bromo-3-indoxylacetate;5-Bromo-3-indolyl Acetate;5-Bromoindoxyl acetate,98%;5-Bromoindoxyl Acetate >
- CBNumber:
- CB2103635
- Molecular Formula:
- C10H8BrNO2
- Molecular Weight:
- 254.08
- MDL Number:
- MFCD00037933
- MOL File:
- 17357-14-1.mol
- MSDS File:
- SDS
- TDS File:
- TDS
Last updated:2026-05-27 23:51:58
| Product description | Number | Pack Size | Price |
| 5-Bromoindoxyl acetate 98% | 374210 | 1g | $388 |
| 5-Bromoindoxyl Acetate >98.0%(HPLC)(N) | A0940 | 100mg | $41 |
| 3-Acetoxy-5-bromoindole Asreported | 260996 | 500mg | $333 |
| 3-Acetoxy-5-bromoindole Asreported | 260996 | 1g | $493 |
| 3-Acetoxy-5-bromoindole Asreported | 260996 | 2g | $668 |
| More product size | |||
| Melting point | 130-132 °C(lit.) |
|---|---|
| storage temp. | Keep in dark place,Inert atmosphere,Room temperature |
| solubility | ethanol: soluble50mg/mL, clear, colorless |
| form | powder to crystal |
| color | White to Purple |
| BRN | 168698 |
| InChI | 1S/C10H8BrNO2/c1-6(13)14-10-5-12-9-3-2-7(11)4-8(9)10/h2-5,12H,1H3 |
| InChIKey | KFTGECHXNQBTNZ-UHFFFAOYSA-N |
| SMILES | CC(=O)Oc1c[nH]c2ccc(Br)cc12 |
| CAS DataBase Reference | 17357-14-1(CAS DataBase Reference) |
| FDA UNII | FBY7EQC6N4 |
| EPA Substance Registry System | 1H-Indol-3-ol, 5-bromo-, acetate (ester) (17357-14-1) |
| UNSPSC Code | 12352100 |
| NACRES | NA.22 |
SAFETY
Risk and Safety Statements
| Symbol(GHS) |  GHS07 |
|---|---|
| Signal word | Warning |
| Hazard statements | H302-H317 |
| Precautionary statements | P280-P305+P351+P338 |
| PPE | Eyeshields, Gloves, type N95 (US) |
| Safety Statements | 22-24/25 |
| WGK Germany | 3 |
| F | 8-10 |
| TSCA | TSCA listed |
| HS Code | 2933998090 |
| Storage Class | 11 - Combustible Solids |
3-ACETOXY-5-BROMOINDOLE price More Price(69)
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Sigma-Aldrich | 374210 | 5-Bromoindoxyl acetate 98% | 17357-14-1 | 1g | $388 | 2026-04-30 | Buy |
| TCI Chemical | A0940 | 5-Bromoindoxyl Acetate >98.0%(HPLC)(N) | 17357-14-1 | 100mg | $41 | 2026-04-30 | Buy |
| Usbiological | 260996 | 3-Acetoxy-5-bromoindole Asreported | 17357-14-1 | 500mg | $333 | 2026-06-03 | Buy |
| Usbiological | 260996 | 3-Acetoxy-5-bromoindole Asreported | 17357-14-1 | 1g | $493 | 2026-06-03 | Buy |
| Usbiological | 260996 | 3-Acetoxy-5-bromoindole Asreported | 17357-14-1 | 2g | $668 | 2026-06-03 | Buy |
3-ACETOXY-5-BROMOINDOLE Chemical Properties,Uses,Production
Uses
5-Bromoindoxyl acetate may be used:
- as esterase substrate to investigate the activity of non-specific esterase in the matrix of developing bovine enamel
- in histochemical studies of the nonspecific esterase of mouse epididymis
- as substrate to investigate the esterase activity in guinea-pig thyroid and mouse epididymis epithelial cells
- in staining procedure for the frozen sections of muscle fixed in buffered formaldehyde
General Description
5-Bromoindoxyl acetate is a halogenated heterocyclic compound. It is widely used as esterase substrate.
Synthesis
Method I.
The 3-hydroxyindole acetate, N-bromosuccinimide and 150 mL of carbon tetrachloride. It was added into 250 mL round bottom flask and refluxed in oil bath for 2 h. The reaction process was monitored by TLC. At the completion of the reaction, the solution changed from dark yellow to light yellow and a white solid (succinimide) was precipitated. The filtrate was withdrawn and washed, and the filtrate was collected and evaporated to obtain 5-bromo-3-hydroxyindole acetate.
Method II.
In a 500 mL single-necked flask, 3-hydroxyindole acetic acid ester was dissolved in tetrahydrofuran solution, N-bromosuccinimide was added in an ice bath, and the reaction was stirred at 0C for 3 h. The reaction was completed. The reaction mixture was poured into 150 mL of ice water and extracted with methyl tert-butyl ether (100 mL4), the organic phases were combined, dried with anhydrous sodium sulfate, and concentrated to obtain 5-bromo-3-hydroxyindole acetate.
3-ACETOXY-5-BROMOINDOLE Preparation Products And Raw materials
Raw materials
Preparation Products
Global( 144)Suppliers
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
| ATK CHEMICAL COMPANY LIMITED | +undefined-21-51877795 | ivan@atkchemical.com | China | 33024 | 60 |
| BOC Sciences | +1-631-485-4226 | inquiry@bocsci.com | United States | 19936 | 58 |
| 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 |
| Zhengzhou Alfa Chemical Co.,Ltd | +8618530059196 | sale04@alfachem.cn | China | 9545 | 58 |
| Hefei TNJ Chemical Industry Co.,Ltd. | +86-0551-65418671 +8618949823763 | sales@tnjchem.com | China | 34563 | 58 |
| Shanghai UCHEM Inc. | +862156762820 +86-13564624040 | sales@myuchem.com | China | 8740 | 58 |
| Dayang Chem (Hangzhou) Co.,Ltd. | +86-0571-88938639 +8617705817739 | info@dycnchem.com | China | 52704 | 58 |
| PT CHEM GROUP LIMITED | +86-85511178; | peter68@ptchemgroup.com | China | 35425 | 58 |
| GIHI CHEMICALS CO.,LIMITED | +86-571-86217390; +8618058761490 | info@gihichemicals.com | China | 49962 | 58 |
View Lastest Price from 3-ACETOXY-5-BROMOINDOLE manufacturers
| Image | Update time | Product | Price | Min. Order | Purity | Supply Ability | Manufacturer | |
|---|---|---|---|---|---|---|---|---|
 |
2020-02-01 | 3-ACETOXY-5-BROMOINDOLE
17357-14-1
|
$3.00 | 1KG | 98% | 100KG | Career Henan Chemical Co |
-
- 3-ACETOXY-5-BROMOINDOLE
17357-14-1
- $3.00
- 98%
- Career Henan Chemical Co
17357-14-1(3-ACETOXY-5-BROMOINDOLE)Related Search:
3-ACETOXY-5-BROMOINDOLE
1-Acetyl-5-bromo-4-chloro-1H-indol-3-yl acetate
5-BROMOINDOXYL DIACETATE
5-BROMO-4-CHLORO-3-INDOLYL ACETATE
1H-INDOL-3-OL
INDOXYL ACETATE
5-Bromoindole
5-BROMO-4-CHLORO-3-INDOLYL BUTYRATE
5-BROMO-4-CHLORO-3-INDOLYL CAPRYLATE
5-BROMO-3-INDOXYL NONANOATE
1of4
acetic acid (5-bromo-1H-indol-3-yl) ester
3-ACETOXY-5-BROMOINDOLE
5-BROMOINDOXYL-3-ACETATE
5-BROMOINDOXYL ACETATE
5-BROMOINDOLYL 3-ACETATE
5-BROMO-1H-INDOL-3-YL ACETATE
1H-Indol-3-ol, 5-bromo-, acetate (ester)
O-ACETYL-5-BROMOINDOXYL
5-BROMOINDOLYL ACETATE
5-BROMOINDOXYL-3-ACETATE 98%
5-BROMOINDOXYLACETATE extrapure AR
3-Acetoxy-5-bromoindole, O-Acetyl-5-bromoindoxyl
3-Acetoxy-5-bromo-1H-indole
5-Bromo-1H-indol-3-ol acetate
5-Bromoindoxyl acetate,98%
5-BroMo-3-indoxyl-3-acetate
1H-Indol-3-ol,5-broMo-, 3-acetate
(5-bromo-1H-indol-3-yl) ethanoate
5-Bromoindoxyl Acetate >
5-Bromo-3-indolyl Acetate
5-Bromo indoxyl acetate, GR 99%
5-Bromo-1H-Indol-3-Ol 3-Acetate
5-Bromo-3-indoxylacetate
17357-14-1
ESTER
Enzymes, Inhibitors, and Substrates
Halogenated Heterocycles
Heterocyclic Building Blocks
Enzyme Substrates
Esterase
Substrates by Enzyme
Indoles
Simple Indoles
Biochemicals and Reagents
Building Blocks
BioChemical
Heterocyclic Compounds
Indoles
Simple Indoles
substrate
