1H-Indole, 4-broMo-5-Methoxy-

1H-Indole, 4-broMo-5-Methoxy- Suppliers list
Company Name: Guangzhou Yuheng Pharmaceutical Technology Co., Ltd
Tel: +8613580539051
Email: joe@yuhengpharm.com
Products Intro: Product Name:4-bromo-5-methoxy-1H-indole
CAS:90858-86-9
Purity:0.97 Package:1KG;25KG
Company Name: KARMEL TECHNOLOGY (HK) CO.,LIMITED
Tel: +8618795957998
Email: karmelhk@126.com
Products Intro: Product Name:1H-Indole, 4-broMo-5-Methoxy-
CAS:90858-86-9
Purity:0.98 Package:1g; 5g; 10g; 25g; 100g
Company Name: Blocksynth Pharmaceutical Technology Co.,Ltd
Tel: 0086-19817745290; +8619817745290
Email: bd@blocksynth.com
Products Intro: Product Name:4-Bromo-5-methoxyindole
CAS:90858-86-9
Purity:98% Package:25KG;USD
Company Name: CR Corporation Limited
Tel: +8613062833949
Email: fred.wen@crcorporation.cn
Products Intro: Product Name:4-bromo-5-methoxy-1H-indole
CAS:90858-86-9
Company Name: Coresyn Pharmatech Co., Ltd.
Tel: +86-571-86626709 +86-18157142896
Email: cbc@coresyn.com
Products Intro: Product Name:4-bromo-5-methoxy-1H-indole
CAS:90858-86-9
Purity:NLT 98% Package:1G;1KG;100KG Remarks:CM31546
1H-Indole, 4-broMo-5-Methoxy- Basic information
Product Name:1H-Indole, 4-broMo-5-Methoxy-
Synonyms:4-Bromo-5-methoxyindole;1H-Indole, 4-broMo-5-Methoxy-
CAS:90858-86-9
MF:C9H8BrNO
MW:226.07
EINECS:
Product Categories:
Mol File:90858-86-9.mol
1H-Indole, 4-broMo-5-Methoxy- Structure
1H-Indole, 4-broMo-5-Methoxy- Chemical Properties
Boiling point 349.2±22.0 °C(Predicted)
density 1.591±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
pka15.77±0.30(Predicted)
AppearanceWhite to yellow Solid
Safety Information
HS Code 2933998090
MSDS Information
1H-Indole, 4-broMo-5-Methoxy- Usage And Synthesis
Synthesis
2-Bromo-4-nitroanisole

5197-28-4

Vinylmagnesium bromide

1826-67-1

1H-Indole, 4-broMo-5-Methoxy-

90858-86-9

Example 12 Synthesis of 4-bromo-5-methoxyindole (XLVI): to a solution of 2-bromo-4-nitroanisole (1.16 g, 5 mmol) in tetrahydrofuran (THF, 10 ml) was slowly added vinylmagnesium bromide (1 M solution in THF, 15 ml) at -40 °C. The reaction mixture was stirred at this temperature for 30 min, followed by a slow warming to -20 °C. Upon completion of the reaction, the reaction was quenched by the addition of saturated ammonium chloride (NH4Cl) solution and subsequently diluted with ether (Et2O). The aqueous layer was extracted twice with ether (Et2O). All organic layers were combined, dried with anhydrous sodium sulfate (Na2SO4), filtered and concentrated. Purification by fast chromatography (eluent: hexane/ethyl acetate) gave 4-bromo-5-methoxyindole (XLVI, 38 mg, 3% yield) as an oil.

References[1] Patent: US2007/123527, 2007, A1. Location in patent: Page/Page column 66-67
1H-Indole, 4-broMo-5-Methoxy- Preparation Products And Raw materials
Raw materials2-Bromo-4-nitroanisole-->Vinylmagnesium bromide
Tag:1H-Indole, 4-broMo-5-Methoxy-(90858-86-9) Related Product Information
4-bromo-5-methyl-1H-pyrrolo[2,3-b]pyridine 4-BROMO-7-FLUOROINDOLE 4-BROMO-6-FLUORO (1H)INDAZOLE 4-BROMO-5-AZAINDOLE NA 4-bromo-5-chloro indole 4-BROMO-7-METHYL-1H-INDOLE 1H-Indole, 4-broMo-5-Methyl-