| Identification | More | [Name]
3-ACETOXY-5-BROMOINDOLE | [CAS]
17357-14-1 | [Synonyms]
3-ACETOXY-5-BROMOINDOLE
5-BROMO-1H-INDOL-3-YL ACETATE
5-BROMOINDOLYL 3-ACETATE
5-BROMOINDOXYL-3-ACETATE
5-BROMOINDOXYL ACETATE
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 | [EINECS(EC#)]
241-387-8 | [Molecular Formula]
C10H8BrNO2 | [MDL Number]
MFCD00037933 | [Molecular Weight]
254.08 | [MOL File]
17357-14-1.mol |
| Safety Data | Back Directory | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [F ]
8-10 | [TSCA ]
TSCA listed | [HS Code ]
2933998090 |
| Hazard Information | Back Directory | [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 reacti |
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J & K SCIENTIFIC LTD.
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18210857532 18210857532 |
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https://www.jkchemical.com |
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Energy Chemical
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400-0056266 |
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www.energy-chemical.com |
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Maya High Purity Chemicals
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