ChemicalBook > CAS DataBase List > 3-ACETOXY-5-BROMOINDOLE

3-ACETOXY-5-BROMOINDOLE

Product Name
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-indolyl Acetate;5-Bromoindoxyl acetate,98%;5-Bromoindoxyl Acetate >3-Acetoxy-5-bromo-1H-indole
CBNumber
CB2103635
Molecular Formula
C10H8BrNO2
Formula Weight
254.08
MOL File
17357-14-1.mol
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3-ACETOXY-5-BROMOINDOLE Property

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
CAS DataBase Reference
17357-14-1(CAS DataBase Reference)
EPA Substance Registry System
1H-Indol-3-ol, 5-bromo-, acetate (ester) (17357-14-1)
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Safety

Safety Statements 
22-24/25
WGK Germany 
3
8-10
HS Code 
2933998090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H317May cause an allergic skin reaction

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
374210
Product name
5-Bromoindoxyl acetate
Purity
98%
Packaging
1g
Price
$425
Updated
2024/03/01
TCI Chemical
Product number
A0940
Product name
5-Bromoindoxyl Acetate
Purity
>98.0%(HPLC)(N)
Packaging
100mg
Price
$35
Updated
2024/03/01
Biosynth Carbosynth
Product number
FA52314
Product name
3-Acetoxy-5-bromoindole
Packaging
250mg
Price
$55
Updated
2021/12/16
Biosynth Carbosynth
Product number
FA52314
Product name
3-Acetoxy-5-bromoindole
Packaging
1g
Price
$150
Updated
2021/12/16
Apolloscientific
Product number
BIB1191
Product name
5-Bromoindolylacetate
Packaging
1g
Price
$182
Updated
2021/12/16
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3-ACETOXY-5-BROMOINDOLE Chemical Properties,Usage,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.

3-ACETOXY-5-BROMOINDOLE Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from 3-ACETOXY-5-BROMOINDOLE manufacturers

Career Henan Chemical Co
Product
3-ACETOXY-5-BROMOINDOLE 17357-14-1
Price
US $3.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
100KG
Release date
2020-01-30

17357-14-1, 3-ACETOXY-5-BROMOINDOLERelated Search:


  • 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 &gt
  • 5-Bromo-3-indolyl Acetate
  • 5-Bromo indoxyl acetate, GR 99%
  • 5-Bromo-1H-Indol-3-Ol 3-Acetate
  • 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