5446-16-2

Basic information

• Product Name: (5-CHLORO-2-METHOXY-PHENYL)-HYDRAZINE HYDROCHLORIDE
• Synonyms: Hydrazine,(5-chloro-2-Methoxyphenyl)-, hydrochloride (1:1);1-(5-CHLORO-2-METHOXYPHENYL)HYDRAZINE HYDROCHLORIDE;(5-CHLORO-2-METHOXY-PHENYL)-HYDRAZINE HYDROCHLORIDE;BIO-FARMA BF001051;4-Chloro-2-hydrazinoanisole hydrochloride, 4-Chloro-2-hydrazino-1-methoxybenzene hydrochloride
• CAS NO: 5446-16-2
• Molecular Formula: C₇H₉ClN₂O*ClH
• Molecular Weight: 209.07
• Mol File: 5446-16-2.mol
• Article Data: 1

Chemical Properties

• Melting Point: 195-196 °C (decomp)
• Boiling Point: 285.7 °C at 760 mmHg
• Flash Point: 126.6 °C
• Appearance: /
• Density: 1.307 g/cm³
• Vapor Pressure: 0.00275mmHg at 25°C
• Refractive Index: 1.619
• CAS DataBase Reference: (5-CHLORO-2-METHOXY-PHENYL)-HYDRAZINE HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: (5-CHLORO-2-METHOXY-PHENYL)-HYDRAZINE HYDROCHLORIDE(5446-16-2)
• EPA Substance Registry System: (5-CHLORO-2-METHOXY-PHENYL)-HYDRAZINE HYDROCHLORIDE(5446-16-2)

Safety Data

• Hazard Codes: Xi,T
• Statements: 25
• Safety Statements: 45
• Hazardous Substances Data: 5446-16-2(Hazardous Substances Data)

Usage

Description

(5-CHLORO-2-METHOXY-PHENYL)-HYDRAZINE HYDROCHLORIDE is an organic compound with the chemical formula C7H8ClN2O?HCl. It is a derivative of hydrazine and features a chlorinated and methoxy-substituted phenyl ring. (5-CHLORO-2-METHOXY-PHENYL)-HYDRAZINE HYDROCHLORIDE is known for its reactivity and is commonly utilized in the synthesis of various organic molecules, particularly those with potential pharmaceutical applications.

Uses

Used in Pharmaceutical Industry:
(5-CHLORO-2-METHOXY-PHENYL)-HYDRAZINE HYDROCHLORIDE is used as a reactant for the preparation of 2-[1-(5-chloro-2-methoxy-phenyl)-5-methyl-1H-pyrazol-4-yl]-5-aryloxadiazoles. These synthesized compounds exhibit antibacterial activity, making them valuable in the development of new antibiotics to combat bacterial infections. (5-CHLORO-2-METHOXY-PHENYL)-HYDRAZINE HYDROCHLORIDE's role in this process is crucial, as it contributes to the formation of the final product's molecular structure, which determines its biological activity and potential therapeutic effects.

InChI:InChI=1/C7H9ClN2O/c1-11-7-3-2-5(8)4-6(7)10-9/h2-4,10H,9H2,1H3

Upstream product

• 95-03-4 5-chloro-2-methoxyaniline 

Downstream Products

• 131197-00-7 4-[2-(5-chloro-2-methoxy-phenyl)-5-methyl-2H-pyrazol-3-yl]-pyridine 
• 131196-99-1 4-[1-(5-chloro-2-methoxy-phenyl)-5-methyl-1H-pyrazol-3-yl]-pyridine 
• 1198352-87-2 ethyl 1-(5-chloro-2-methoxyphenyl)-5-methyl-1H-pyrazole-4-carboxylate 
• 1555700-00-9 ethyl 4-chloro-7-methoxy-3-methyl-1-(2-nitrophenyl)-2,3-dihydro-1H-indole-3-carboxylate 
• 1555700-01-0 ethyl 1-(2-aminophenyl)-4-chloro-7-methoxy-3-methyl-2,3-dihydro-1H-indole-3-carboxylate 
• 1555700-74-7 ethyl 4-chloro-7-methoxy-3-methyl-1-[2-({[4-(trifluoromethoxy)-phenyl]carbamoyl}amino)phenyl]-2,3-dihydro-1H-indole-3-carboxylate 
• 1555694-30-8 ethyl 4-chloro-7-hydroxy-3-methyl-1-[2-({[4-(trifluoromethoxy)phenyl]carbamoyl}amino)phenyl]-2,3-dihydro-1H-indole-3-carboxylate 

Relevant articles and documents

7-HYDROXY-SPIROPIPIPERIDINE INDOLINYL ANTAGONISTS OF P2Y1 RECEPTOR

The present invention provides compounds of Formula (I): as defined in the specification and compositions comprising any of such novel compounds. These compounds are antagonists of Ρ2Y1 receptor and may be used as medicaments in the treatment and/or prophylaxis of thromboembolic disorders.