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5-Bromo-7-methyl-1H-indole

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Company Name: Alchem Pharmtech,Inc.
Tel: 8485655694
Email: sales@alchempharmtech.com
Products Intro: Product Name:5-Bromo-7-methyl-1H-indole
CAS:15936-81-9
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-43023
Company Name: career henan chemical co
Tel: +86-0371-86658258 15093356674;
Email: factory@coreychem.com
Products Intro: Product Name:5-Bromo-7-methyl-1H-indole
CAS:15936-81-9
Purity:>=99% Package:1.8KG;9.8USD
Company Name: Fuxin Pharmaceutical
Tel: +86-021-021-50872116 +8613122107989
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Products Intro: Product Name:5-Bromo-7-methyl-Indole
CAS:15936-81-9
Purity:99% Package:1kg; 25kg; or larger package as required
Company Name: KARMEL TECHNOLOGY (HK) CO.,LIMITED
Tel: +8618795957998
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Products Intro: Product Name:5-Bromo-7-methyl-1H-indole
CAS:15936-81-9
Purity:0.98 Package:1g; 5g; 10g; 25g; 100g
Company Name: Dayang Chem (Hangzhou) Co.,Ltd.
Tel: 571-88938639 +8617705817739
Email: info@dycnchem.com
Products Intro: Product Name:1H-Indole, 5-bromo-7-methyl-
CAS:15936-81-9
Purity:0.95&0.99 Package:0.1KG;1KG;1000KG Remarks:Factory Supply

5-Bromo-7-methyl-1H-indole manufacturers

5-Bromo-7-methyl-1H-indole Basic information
Product Name:5-Bromo-7-methyl-1H-indole
Synonyms:5-Bromo-7-methyl-1H-indole;5-BroMo-7-Methylindole;1H-Indole, 5-bromo-7-methyl-;EOS-61850;7-methyl-5-bromo-1H-indole
CAS:15936-81-9
MF:C9H8BrN
MW:210.07
EINECS:
Product Categories:
Mol File:15936-81-9.mol
5-Bromo-7-methyl-1H-indole Structure
5-Bromo-7-methyl-1H-indole Chemical Properties
Boiling point 165 °C(Press: 0.1 Torr)
density 1.503 g/mL at 25 °C
refractive index n20/D1.648
Fp >110℃
storage temp. Sealed in dry,Room Temperature
form Solid or semi-solid or lump or liquid
pka16.34±0.30(Predicted)
Safety Information
Hazard Codes Xn
Risk Statements 22-37/38-41
Safety Statements 26-39
WGK Germany 3
MSDS Information
5-Bromo-7-methyl-1H-indole Usage And Synthesis
Synthesis5-Bromo-7-methyl-1H-indole is synthesised from 4-bromo-6-(trimethylsilylacetylenyl)-2-methylaniline by reacting with potassium tert-butyrate and sodium hydride in the presence of inert gas. The steps are as follows:
Add sodium hydride (2.64g, 0.11mol) and DMF (70mL) to a 250ml three-necked flask at room temperature and under nitrogen protection.Stir and dissolve; a solution of the compound of formula IV (14g, 0.05mol) dissolved in DMF (30mL) is slowly added dropwise to the potassium tert-butoxide solution. After the addition, the reaction system was heated to 60 degrees and kept for 2 hours. After the reaction was completed, the reaction solution was poured into ice water, extracted with methyl tert-butyl ether, and washed with sodium bicarbonate aqueous solution and brine in turn.It was then dried over anhydrous sodium sulfate, filtered, and concentrated. The crude product is purified by silica gel column chromatography to obtain the compound of 5-bromo-7-methylindole. Yield: 8.36 g, yield: 80%.
5-Bromo-7-methyl-1H-indole synthesis
5-Bromo-7-methyl-1H-indole Preparation Products And Raw materials
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