6310-14-1

Basic information

• Product Name: (Z)-1-(4-methoxyphenyl)ethylidenehydrazine
• Synonyms: (Z)-1-(4-methoxyphenyl)ethylidenehydrazine
• CAS NO: 6310-14-1
• Molecular Formula: C₉H₁₂N₂O
• Molecular Weight: 164.2
• Mol File: 6310-14-1.mol
• Article Data: 20

Chemical Properties

• Boiling Point: 286.2°C at 760 mmHg
• Flash Point: 126.9°C
• Appearance: /
• Density: 1.05g/cm³
• Vapor Pressure: 0.00268mmHg at 25°C
• Refractive Index: 1.524
• CAS DataBase Reference: (Z)-1-(4-methoxyphenyl)ethylidenehydrazine(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-1-(4-methoxyphenyl)ethylidenehydrazine(6310-14-1)
• EPA Substance Registry System: (Z)-1-(4-methoxyphenyl)ethylidenehydrazine(6310-14-1)

Safety Data

• Hazardous Substances Data: 6310-14-1(Hazardous Substances Data)

Usage

Description

(Z)-1-(4-methoxyphenyl)ethylidenehydrazine, also known as 4-methoxyphenyl ethylidene hydrazine, is an organic chemical compound with the molecular formula C9H12N2O. It features a hydrazine functional group and a methoxyphenyl group, making it a versatile compound for various applications in chemical research and the pharmaceutical industry. Due to its potential hazards to human health, including skin, eye, and respiratory irritation, it is crucial to handle this compound with caution.

Uses

Used in Chemical Research:
(Z)-1-(4-methoxyphenyl)ethylidenehydrazine is used as a research compound for [application reason] in the field of chemical research. Its unique structure allows for further exploration and development of new chemical reactions and processes.
Used in Pharmaceutical Industry:
(Z)-1-(4-methoxyphenyl)ethylidenehydrazine is used as a starting material or intermediate for [application reason] in the pharmaceutical industry. Its potential applications may include the development of new drugs or the enhancement of existing ones, depending on the specific context and requirements.
Please note that the "application reason" should be filled in with the specific purpose or benefit of using (Z)-1-(4-methoxyphenyl)ethylidenehydrazine in each application area. The provided materials do not give explicit reasons for its use, so this information would need to be researched or provided by an expert in the field.

InChI:InChI=1/C9H12N2O/c1-7(11-10)8-3-5-9(12-2)6-4-8/h3-6H,10H2,1-2H3/b11-7-

Upstream product

• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 2632-13-5 2-Bromo-4'-methoxyacetophenone 
• 92435-63-7 2-(4-chlorophenoxy)-1-(4-methoxyphenyl)ethan-1-one 
• 768-60-5 4-methoxyphenylacetylen 
• 5757-98-2 p-Methoxyacetophenone N,N-dimethylhydrazone 

Downstream Products

• 29443-55-8 1-(1-iodoethenyl)-4-methoxybenzene 
• 121-98-2 methyl 4-methoxybenzoate 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 94-30-4 ethyl 4-methoxybenzoate 
• 89752-31-8 7-(4-Methoxy-phenyl)-7-methyl-2,3a,5-triphenyl-3,3a-dihydro-pyrazolo[1,5-c][1,3]oxazine 
• 70078-14-7 1-(1-diazoethyl)-4-methoxybenzene 
• 65124-88-1 1-(4-methoxyphenyl)ethanone <1-(4-methoxyphenyl)ethylidene>hydrazone 
• 73104-88-8 1-(p-methoxyphenyl)ethyl acetate 
• 77525-91-8 1-methoxy-4-(1-methoxy-ethyl)-benzene 
• 21399-34-8 1,2-bis(1-(4-methoxyphenyl)ethylidene)hydrazine 
• 1536278-44-0 6-methoxy-3-methyl-1,2-diphenyl-1H-indene 
• 895-37-4 4,4'-(but-2-ene-2,3-diyl)bis(methoxybenzene) 
• 6938-38-1 4-methoxy-benzoic acid isopropyl ester 
• 1269772-83-9 (4-fluorophenyl)(1-(4-methoxyphenyl)ethyl)sulfane 

Relevant articles and documents

Near-perfect dipole parallel-alignment in the highly anisotropic crystal structure of 4-iodoacetophenone-(4-methoxyphenylethylidene) hydrazone

The title compound crystallizes in the space group Pna2(1) with cell parameters a = 6.4606(3), b = 7.2155(3) and c = 33.5878(16) A. The azine shows a gauche conformation about the N - N bond and there is an angle of 58.1° between the benzene rings of each azine. This conformation allows for two intermolecular arene-arene T-contacts between pairs of benzene rings. The characteristic structural motif features T-contact formation between like-substituted arene rings and this architecture results in a highly dipole-parallel aligned lattice. All azines are perfectly colinear within each layer and the orientations of the azines in different layers are nearly the same. The surfaces of the layers exhibit a quadrilateral kite-shaped arrangement of I-atoms and of OCH3-substituents. The layers pack such that the OCH3 - carbon atoms are placed above the interstices between the I-atoms in the adjacent layer.

Sequential Cleavage of Lignin Systems by Nitrogen Monoxide and Hydrazine

The cleavage of representative lignin systems has been achieved in a metal-free two-step sequence first employing nitrogen monoxide for oxidation followed by hydrazine for reductive C?O bond scission. In combining nitrogen monoxide and lignin, the newly developed valorization strategy shows the particular feature of starting from two waste materials, and it further exploits the attractive conditions of a Wolff-Kishner reduction for C?O bond cleavage for the first time. (Figure presented.).

Synthesis and Catalytic Benefits of Tetranuclear Gold(I) Complexes with a C4-Symmetric Tetratriazol-5-ylidene

The facile preparation of a C4-symmteric tetratriazolium salt and its subsequent metalation to generate a series of tetranuclear mesoionic carbene gold(I) complexes is presented. The complete structural characterization of the metallic carbenes