4-Bromoindole

4-Bromoindole Basic information

Product Name:	4-Bromoindole
Synonyms:	4-BROMO-1H-INDOLE,4-BROMOINDOLE;4-BROMO-1H-INDAZOLE;4-BROMO-INDOLE pure;4-Bromoindole ,95%;4-Bromo-1H-indole , TECH;1H-Indole,4-broMo-;4-Bromoindole 96%;4-BROMOINDOLE
CAS:	52488-36-5
MF:	C8H6BrN
MW:	196.04
EINECS:	610-851-5
Product Categories:	Simple Indoles;Pyrroles & Indoles;Indole Derivatives;Halogenated Heterocycles;Heterocyclic Building Blocks;IndolesBuilding Blocks;blocks;Indole/indoline/oxindole;Heterocycles series;Halides;Pyrroles & Indoles;Indole;Indoles;Heterocycle-Indole series;Bromides;IndolesOxindoles;Indoles and derivatives;pharmacetical
Mol File:	52488-36-5.mol

4-Bromoindole Chemical Properties

Melting point	17 °C
Boiling point	283-285 °C (lit.)
density	1.563 g/mL at 25 °C (lit.)
refractive index	n20/D 1.655(lit.)
Fp	230 °F
storage temp.	Keep in dark place,Sealed in dry,Room Temperature
solubility	Chloroform (Sparingly), DMSO (Slightly) Ethyl Acetate
form	Oil
pka	16.07±0.30(Predicted)
Specific Gravity	1.563
color	Pale Yellow to Yellow
Water Solubility	Not miscible in water.
Sensitive	Light Sensitive
BRN	114891
InChIKey	GRJZJFUBQYULKL-UHFFFAOYSA-N
CAS DataBase Reference	52488-36-5(CAS DataBase Reference)

Safety Information

Hazard Codes	Xi
Risk Statements	36/37/38
Safety Statements	26-36-37/39
WGK Germany	3
Hazard Note	Keep Cold/Light Sensitive
HazardClass	IRRITANT, KEEP COLD
HS Code	29339990

MSDS Information

Provider	Language
ACROS	English
SigmaAldrich	English
ALFA	English

4-Bromoindole Usage And Synthesis

Chemical Properties	Clear yellowish-green or dark brown liquid
Uses	4-Bromoindole is a potential inhibitor of GSK-3. It is also used as pharmaceutical intermediates.
Uses	4-Bromoindole may be used to synthesize: clavicipitic acid, an ergot alkaloid 4-bromodehydrotryptophan 3-indolylacetonitrile derivative marine alkaloid dictyodendrin B

4-Bromoindole Preparation Products And Raw materials

Raw materials	4-Fluorobenzeneboronic acid
Preparation Products	Indole-4-boronic acid-->4-Bromoindole-3-carboxaldehyde-->4-BROMO-1-METHYL-1H-INDOLE-->1H-Indole-3-aceticacid,4-bromo-(9CI)-->1-benzyl-4-bromo-indole-->1-(4-bromo-1H-indol-3-yl)ethanone-->N-pivaloyl-4-bromoindole-->4-bromo-1-tosyl-1H-indole-3-carbaldehyde-->Ethyl 1H-indole-4-carboxylate

7-Bromoindole 5-BROMOINDOLE-2-CARBOXYLIC ACID 3-BROMOINDOLE-2-CARBOXYLIC ACID 4-BROMOINDOLE-2,3-DIONE 4-BROMOINDOLE, N-BOC PROTECTED,4-BROMOINDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER 1-ACETYL-5-BROMOINDOLE 2-[2'-NITROPHENYLSULFENYL]-3-METHYL-3-BROMOINDOLE 4-Bromo-2-indolecarboxylic acid 7-AMINO-5-BROMOINDOLE 5-BROMOINDOLE-3-ACETAMIDE 5-BROMOINDOLE 5-BROMOINDOLE-3-ACETIC ACID 4-BENZYLOXY-3-BROMOINDOLE, N-BOC PROTECTED,4-BENZYLOXY-3-BROMOINDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER 7-Bromo-1H-indole, N-BOC protected 5-BROMOINDOLE-3-CARBOXYLIC ACID 6-Bromoisatinic anhydride 6-bromoindole-3-carboxylic acid 6-Bromo-1,3-dihydro-2H-indol-2-one

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