21968-29-6

Basic information

• Product Name: Benzaldehyde, 2-methoxy-, phenylhydrazone
• CAS NO: 21968-29-6
• Molecular Formula: C14H14N2O
• Molecular Weight: 226.278
• Mol File: 21968-29-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 2-methoxy-, phenylhydrazone(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 2-methoxy-, phenylhydrazone(21968-29-6)
• EPA Substance Registry System: Benzaldehyde, 2-methoxy-, phenylhydrazone(21968-29-6)

Safety Data

• Hazardous Substances Data: 21968-29-6(Hazardous Substances Data)

Upstream product

• 100-63-0 phenylhydrazine 
• 135-02-4 ortho-anisaldehyde 
• 62-53-3 aniline 
• 59-88-1 phenylhydrazine hydrochloride 

Downstream Products

• 62164-45-8 1,5-diphenyl-3-(o-methoxyphenyl)formazane 
• 135-02-4 ortho-anisaldehyde 
• 1310486-85-1 1-benzyl-2-(2-methoxyphenyl)-1H-benzo[d]imidazole 
• 380219-54-5 2-(2-methoxybenzylidene)-1-benzyl-1-phenylhydrazine 
• 58162-87-1 14-(2-methoxyphenyl)-14H-dibenzo[a,j]xanthene 
• 1376268-49-3 3,5-bis(2-methoxyphenyl)-1-phenyl-1H-1,2,4-triazole 
• 97783-04-5 (2-Methoxy-phenyl)-phenylazo-methyl-hydroperoxide 

Relevant articles and documents

Sequential [3+2] annulation reaction of prop-2-ynylsulfonium salts and hydrazonyl chlorides: Synthesis of pyrazoles containing functional motifs

A novel sequential [3+2] annulation reaction has been developed using prop-2-ynylsulfonium salts and hydrazonyl chlorides, affording a series of pyrazoles with functional motifs that can be post modified in the preparation of various drugs or drug candidates. Further transformation and gram-scale operations could also be achieved efficiently. This journal is

O-methoxy phenylhydrazone dicaryon metal complex and preparation method and application thereof

The invention provides an o-methoxy phenylhydrazone dicaryon metal complex, a preparation method thereof. The complex is used as a catalyst for preparing high-molecular-weight polyethylene. The complex is obtained through the method including the steps th

Copper-mediated synthesis of substituted 2-aryl-N-benzylbenzimidazoles and 2-arylbenzoxazoles via C-H functionalization/C-N/C-O bond formation

An efficient method for the transformation of N-benzyl bisarylhydrazones and bisaryloxime ethers to functionalized 2-aryl-N-benzylbenzimidazoles and 2-arylbenzoxazoles is described. The protocol involves a copper(II)-mediated cascade C-H functionalization/C-N/C-O bond formation under neutral conditions. Substrates having either electron-donating or -withdrawing substituents undergo the cyclization to afford the target heterocycles at moderate temperature.