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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
Molecular Weight:
254.08
MDL Number:
MFCD00037933
MOL File:
17357-14-1.mol
MSDS File:
SDS
Last updated:2023-04-23 13:52:06

3-ACETOXY-5-BROMOINDOLE Properties

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)
FDA UNII FBY7EQC6N4
EPA Substance Registry System 1H-Indol-3-ol, 5-bromo-, acetate (ester) (17357-14-1)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H317
Precautionary statements  P280-P305+P351+P338
Safety Statements  22-24/25
WGK Germany  3
8-10
HS Code  2933998090

3-ACETOXY-5-BROMOINDOLE price More Price(28)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 374210 5-Bromoindoxyl acetate 98% 17357-14-1 1g $425 2024-03-01 Buy
TCI Chemical A0940 5-Bromoindoxyl Acetate >98.0%(HPLC)(N) 17357-14-1 100mg $35 2024-03-01 Buy
Biosynth Carbosynth FA52314 3-Acetoxy-5-bromoindole 17357-14-1 250mg $55 2021-12-16 Buy
Biosynth Carbosynth FA52314 3-Acetoxy-5-bromoindole 17357-14-1 1g $150 2021-12-16 Buy
Apolloscientific BIB1191 5-Bromoindolylacetate 17357-14-1 1g $182 2021-12-16 Buy
Product number Packaging Price Buy
374210 1g $425 Buy
A0940 100mg $35 Buy
FA52314 250mg $55 Buy
FA52314 1g $150 Buy
BIB1191 1g $182 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.

10075-50-0
3240-34-4
17357-14-1
Synthesis of 3-ACETOXY-5-BROMOINDOLE from 5-Bromoindole and (Diacetoxyiodo)benzene

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

Global( 134)Suppliers
Supplier Tel Email Country ProdList Advantage
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
Chongqing Chemdad Co., Ltd
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PT CHEM GROUP LIMITED
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GIHI CHEMICALS CO.,LIMITED
+8618058761490 info@gihichemicals.com China 49999 58

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

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
3-ACETOXY-5-BROMOINDOLE pictures 2020-02-01 3-ACETOXY-5-BROMOINDOLE
17357-14-1
US $3.00 / KG 1KG 98% 100KG Career Henan Chemical Co

3-ACETOXY-5-BROMOINDOLE Spectrum

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 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