2154-24-7

Basic information

• Product Name: (2-MORPHOLIN-4-YL-ETHYL)-HYDRAZINE
• Synonyms: (2-MORPHOLIN-4-YL-ETHYL)-HYDRAZINE;1-(2-morpholinoethyl)hydrazine
• CAS NO: 2154-24-7
• Molecular Formula: C₆H₁₅N₃O
• Molecular Weight: 145.2
• Mol File: 2154-24-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 125 °C(Press: 12 Torr)
• Appearance: /
• Density: 1.050 g/cm3
• PKA: 8.19±0.70(Predicted)
• CAS DataBase Reference: (2-MORPHOLIN-4-YL-ETHYL)-HYDRAZINE(CAS DataBase Reference)
• NIST Chemistry Reference: (2-MORPHOLIN-4-YL-ETHYL)-HYDRAZINE(2154-24-7)
• EPA Substance Registry System: (2-MORPHOLIN-4-YL-ETHYL)-HYDRAZINE(2154-24-7)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 2154-24-7(Hazardous Substances Data)

Usage

General Description

(2-Morpholin-4-yl-ethyl)-hydrazine is a chemical compound with the molecular formula C6H14N4O. It is a hydrazine derivative, which is a class of organic compounds containing a functional group with the formula R2N-NH2. (2-MORPHOLIN-4-YL-ETHYL)-HYDRAZINE has a morpholine ring and an ethyl group attached to a hydrazine moiety. It has potential applications in pharmaceuticals and agrochemicals, and it may also be used as a chemical intermediate in synthesis. Additionally, hydrazine derivatives like (2-morpholin-4-yl-ethyl)-hydrazine have been studied for their potential biological activity and toxicological properties.

Upstream product

• 3647-69-6 4-(2-chloroethyl)morpholine hydrochride 
• 89583-07-3 N-(2-bromoethyl)morpholine 
• 3240-94-6 N-(2-chlorethyl)morpholine 

Downstream Products

• 1099657-54-1 C₁₉H₂₅ClN₆O₂ 
• 51244-57-6 3-methyl-6-(2-morpholin-4-yl-ethyl)-4-phenyl-6H-isoxazolo[3,4-d]pyridazin-7-one 
• 51313-42-9 6-(2-morpholin-4-yl-ethyl)-4-phenyl-6H-isoxazolo[3,4-d]pyridazin-7-one 
• 21769-53-9 3-(2-morpholin-4-yl-ethyl)-5-phenyl-3,4-diaza-bicyclo[4.1.0]hept-4-en-2-one 
• 22139-58-8 3-(3,4-dihydroxy-phenyl)-acrylic acid N'-(2-morpholin-4-yl-ethyl)-hydrazide 
• 29285-75-4 6-(2-hydroxy-phenyl)-4-methyl-2-(2-morpholin-4-yl-ethyl)-2H-pyridazin-3-one 
• 29242-44-2 6-(3-bromo-phenyl)-4-methyl-2-(2-morpholin-4-yl-ethyl)-2H-pyridazin-3-one 
• 29242-45-3 6-(4-bromo-phenyl)-4-methyl-2-(2-morpholin-4-yl-ethyl)-2H-pyridazin-3-one 
• 49869-19-4 2-(2-morpholin-4-yl-ethyl)-8-phenyl-4,5,6,7-tetrahydro-2H-[1,2]diazocin-3-one 
• 33048-50-9 2-(2-morpholin-4-yl-ethyl)-4-phenyl-2H-phthalazin-1-one 

Relevant articles and documents

2-Pyrazolin-5-ones bearing a basic dialkylaminoalkyl substituent at the N1-position: Preparation and NMR spectroscopic investigations

2-Pyrazolin-5-ones (= tautomers to 5-hydroxypyrazols) bearing dialkylaminoyalkyl substituents at the ring nitrogen atom N-1 are prepared from the corresponding hydrazines and beta-ketoesters. Detailed NMR spectroscopic investigations (1H,

3-[1-(2-Benzoxazolyl)hydrazino]propanenitrile derivatives: Inhibitors of immune complex induced inflammation

3-[1-(2-Benzoxazolyl)hydrazino]propanenitrile derivatives were evaluated in the dermal and pleural reverse passive Arthus reactions in the rat. In the pleural test these compounds were effective in reducing exudate volume and accumulation of white blood cells. This pattern of activity was similar to that of hydrocortisone and different from that of indomethacin. The structural requirements for inhibiting the Arthus reactions were studied by systematic chemical modification of 1. These structure-activity relationship studies revealed that nitrogen 1' of the hydrazino group is essential for activity and must be electron rich, whereas chemical modifications of other sites of 1 had only a modest effect on activity.