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P-BROMOPHENYL HYDRAZINE

  • CAS:589-21-9
  • purity:99%
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Details

Manufacturer supply top purity P-BROMOPHENYL HYDRAZINE 589-21-9 with ISO standards

  • Molecular Formula: C6H7BrN2
  • Molecular Weight: 187.039
  • Vapor Pressure: 0.00278mmHg at 25°C 
  • Melting Point: 102-104 °C 
  • Refractive Index: 1.68 
  • Boiling Point: 285.6 °C at 760 mmHg 
  • PKA: 4.93±0.20(Predicted) 
  • Flash Point: 126.5 °C 
  • PSA: 38.05000 
  • Density: 1.666 g/cm3 
  • LogP: 2.50800 

P-BROMOPHENYL HYDRAZINE(Cas 589-21-9) Usage

Purification Methods

Crystallise the hydrazine from H2O. The hydrochloride crystallises from EtOH/H2O with m 213-214o, and the tosylate has m 212o (from EtOH). [Beilstein 15 H 434, 15 I 117, 15 II 160, 15 III 289, 15 IV 282.]

General Description

P-Bromophenyl hydrazine is a key intermediate used in the synthesis of eletriptan via Fischer indole cyclization. Its preparation involves the reduction of p-bromophenyldiazonium salts, optimized using L-ascorbic acid to enhance efficiency and sustainability. P-BROMOPHENYL HYDRAZINE serves as a crucial building block in the streamlined, cost-effective, and environmentally friendly production of eletriptan, demonstrating its importance in pharmaceutical synthesis.

InChI:InChI=1/C6H7BrN2/c7-5-1-3-6(9-8)4-2-5/h1-4,9H,8H2

589-21-9 Relevant articles

NOVEL COMPOUNDS AS NADPH OXIDASE INHIBITORS

-

Paragraph 0291; 0292, (2020/04/09)

The present invention is related to new ...

Lewis Acid Catalyzed Annulation of Cyclopropane Carbaldehydes and Aryl Hydrazines: Construction of Tetrahydropyridazines and Application Toward a One-Pot Synthesis of Hexahydropyrrolo[1,2- b]pyridazines

Dey, Raghunath,Kumar, Pankaj,Banerjee, Prabal

, p. 5438 - 5449 (2018/05/28)

In this report, a facile synthesis of te...

5-Bromo-1-(4-chlorobenzyl)-1h-indole-2-carboxamides as new potent antibacterial agents

Mane, Yogesh D.,Patil, Smita S.,Biradar, Dhanraj O.,Khade, Bhimrao C.

, p. 327 - 332 (2018/11/27)

Ten 5-bromoindole-2-carboxamides were sy...

Design, synthesis, and antimicrobial activity of novel 5-substituted indole-2-carboxamide derivatives

Mane, Yogesh D.,Sarnikar, Yuvaraj P.,Surwase, Santosh M.,Biradar, Dhanraj O.,Gorepatil, Pratapsinha B.,Shinde, Vishnu S.,Khade, Bhimrao C.

, p. 1253 - 1275 (2017/02/10)

Abstract: A series of novel, bioactive 5...

589-21-9 Process route

4-bromophenylhydrazine hydrochloride
622-88-8,41931-18-4

4-bromophenylhydrazine hydrochloride

(4-bromophenyl)hydrazine
589-21-9

(4-bromophenyl)hydrazine

Conditions
Conditions Yield
With sodium carbonate; In dichloromethane; water;
With sodium hydroxide; In tetrahydrofuran; diethyl ether; water; at 0 - 20 ℃; for 1h;
With sodium hydroxide; In tetrahydrofuran; water; for 0.5h;
4.45 g
With ammonium hydroxide; at 0 ℃;
With potassium carbonate; In water; at 20 ℃; for 0.25h;
With potassium carbonate; In water; at 20 ℃; for 0.25h; Inert atmosphere;
N-(4-bromophenyl)-nitramine
412328-47-3

N-(4-bromophenyl)-nitramine

(4-bromophenyl)hydrazine
589-21-9

(4-bromophenyl)hydrazine

Conditions
Conditions Yield
With hydrogenchloride; tin(ll) chloride; In water; for 4h; Cooling with ice;
85%

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