1046784-61-5

Basic information

• Product Name: 5-chloro-3-ethyl-1-phenyl-1H-pyrazole-4-carbaldehyde
• Synonyms: 5-chloro-3-ethyl-1-phenyl-1H-pyrazole-4-carbaldehyde
• CAS NO: 1046784-61-5
• Molecular Weight: 234.685
• Mol File: 1046784-61-5.mol

Chemical Properties

• CAS DataBase Reference: 5-chloro-3-ethyl-1-phenyl-1H-pyrazole-4-carbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 5-chloro-3-ethyl-1-phenyl-1H-pyrazole-4-carbaldehyde(1046784-61-5)
• EPA Substance Registry System: 5-chloro-3-ethyl-1-phenyl-1H-pyrazole-4-carbaldehyde(1046784-61-5)

Safety Data

• Hazardous Substances Data: 1046784-61-5(Hazardous Substances Data)

Upstream product

• 68-12-2 N,N-dimethyl-formamide 
• 92753-34-9 2-phenyl-5-ethyl-2,4-dihydro-3H-pyrazol-3-one 
• 4949-44-4 ethyl propanoylacetate 
• 100-63-0 phenylhydrazine 

Downstream Products

• 1660146-13-3 2-cyano-3-(3-ethyl-1-phenyl-5-pyrrolidino-1H-pyrazol-4-yl)acrylamide 
• 1660146-18-8 5-cyano-3-ethyl-1-phenyl-4,5,5a,6,7,8-hexahydro-1H-pyrazolo[3,4-e]indolizine-5-carboxamide 
• 1660146-09-7 3-ethyl-1-phenyl-5-pyrrolidino-1H-pyrazole-4-carbaldehyde 

Relevant articles and documents

Synthesis of Selenopyrano[2,3- c ]pyrazol-4(1 H)-ones and Their C-H Activation

We disclose the synthesis of selenopyrano[2,3- c ]pyrazol-4(1 H)-ones and their aryl derivatives for the first time by using selenopyran ring formation via an in situ-generated selenide that reacts directly with α-halo-β-ynone-bearing substituted pyrazole

A novel synthetic method of organoselenum compounds

The present application can synthesize a selenopyrano pyrazolone derivative, one of an organic selenium compound, in a simple and excellent yield. Provided is a synthesis method of an organic selenium compound which is eco-friendly at low temperature and

Synthesis of some novel pyrazolopyridooxazine, pyrazoloquinolizines, pyrazoloindolizine and pyrazolopyranopyrimidinone derivatives

Different pyrazolone derivatives were prepared as starting materials for the synthesis of pyrazolopyridooxazine, pyrazoloquinolizines, pyrazoloindolizine, 1,4-oxazinopyrazolines and pyrazolopyranopyrimidinone derivatives via reactions with different reagents applying the one pot multicomponent reaction using microwave and ultrasound irradiation in some cases.