62646-04-2

Basic information

• Product Name: Hydrazine, 1-[(4-chlorophenyl)Methyl]-1-(4-Methoxyphenyl)-
• Synonyms: Hydrazine, 1-[(4-chlorophenyl)Methyl]-1-(4-Methoxyphenyl)-;1-(4-Chlorobenzyl)-1-(4-methoxyphenyl)hydrazine
• CAS NO: 62646-04-2
• Molecular Formula: C₁₄H₁₅ClN₂O
• Molecular Weight: 262.7347
• Mol File: 62646-04-2.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 427.6±35.0 °C(Predicted)
• Appearance: /
• Density: 1.243±0.06 g/cm3(Predicted)
• PKA: 4.67±0.50(Predicted)
• CAS DataBase Reference: Hydrazine, 1-[(4-chlorophenyl)Methyl]-1-(4-Methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Hydrazine, 1-[(4-chlorophenyl)Methyl]-1-(4-Methoxyphenyl)-(62646-04-2)
• EPA Substance Registry System: Hydrazine, 1-[(4-chlorophenyl)Methyl]-1-(4-Methoxyphenyl)-(62646-04-2)

Safety Data

• Hazardous Substances Data: 62646-04-2(Hazardous Substances Data)

Upstream product

• 60-29-7 diethyl ether 
• 19501-58-7 4-methoxyphenylhydrazine hydrochloride 
• 104-83-6 1-Chloro-4-(chloromethyl)benzene 

Downstream Products

• 144174-40-3 (R)-2-[1-(4-Chloro-benzyl)-2-(3-cyano-2,2-dimethyl-propyl)-5-methoxy-1H-indol-3-ylsulfanyl]-propionic acid 
• 20955-94-6 1-[(4-chlorophenyl)methyl]-1-(4-methoxyphenyl)-hydrazine hydrochloride 
• 148929-09-3 3-[1-(4-chlorobenzyl)-5-(6-chloropyrid-2-ylmethoxy)-3-(1,1-dimethylethylthio)indol-2-yl]-2,2-dimethylpropionic acid 
• 154325-78-7 ethyl 3-[1-(4-chlorobenzyl)-3-(1,1-dimethylethylthio)-5-(pyrid-3-ylmethoxy)indol-2-yl]-2,2-dimethylpropionate 
• 149167-98-6 3-[1-(4-chlorobenzyl)-3-(1,1-dimethylethylthio)-5-(thiazol-4-ylmethoxy)indol-2-yl]-2,2-dimethylpropionic acid 
• 148929-01-5 3-[1-(4-chlorobenzyl)-3-(1,1-dimethylethylthio)-5-(pyrid-2-ylmethoxy)indol-2-yl]-2,2-dimethylpropionic acid 
• 148693-71-4 3-[1-(4-Chlorobenzyl)-3-(t-butylthio)-5-hydroxyindol-2-yl]-2,2-dimethylpropanoic acid 

Relevant articles and documents

COMPOSITIONS AND TREATMENTS COMPRISING 5-LIPOXYGENASE-ACTIVATING PROTEIN INHIBITORS AND NITRIC OXIDE MODULATORS

Disclosed herein are compositions and compounds that combine an inhibitor of 5-lipoxygenase activating protein (FLAP) and a modulator of NO levels in a mammal. The NO modulator can be an agent that induces the production of NO in a mammal, or can be an ag

INDOLE IMINOOXY DERIVATIVES WHICH INHIBIT LEUKOTRIENE BIOSYNTHESIS

Compounds of the structure where A1 is alkylene or cycloalkylene; A2 is a valence bond, alkylene, or cycloalkylene; R1 is selected from hydrogen, alkylthio, optionally substituted phenylthio, optionally substituted phenylalkylthio, optionally substituted

Friedel-Crafts Cyclization of 2-(3-Indolylthio)propionic Acids. An Unusual Rearrangement Leading to 4-Sulfur-Substituted Tricyclic Indoles

The intramolecular Friedel-Crafts acylation of 2-(3-indolylthio)propionic acid 1 has been found to undergo an unprecedented rearrangement to provide a novel tricyclic indole having the sulfur substituted on C-4 rather than on the expected C-3.A mechanism for its formation is proposed.This rearrangement also proceeded with good optical retention when a chiral substrate was used.Key Words: Friedel-Crafts acylation; rearrangement; tricyclic indoles; 4-thio-indoles; thiopyranoindoles.