851753-68-9

Basic information

• Product Name: 4-(2-formyl-4-methyl-phenyl)-piperazine-1-carboxylic acid tert-butyl ester
• Synonyms: 4-(2-formyl-4-methyl-phenyl)-piperazine-1-carboxylic acid tert-butyl ester
• CAS NO: 851753-68-9
• Molecular Weight: 304.389
• Mol File: 851753-68-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-(2-formyl-4-methyl-phenyl)-piperazine-1-carboxylic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2-formyl-4-methyl-phenyl)-piperazine-1-carboxylic acid tert-butyl ester(851753-68-9)
• EPA Substance Registry System: 4-(2-formyl-4-methyl-phenyl)-piperazine-1-carboxylic acid tert-butyl ester(851753-68-9)

Safety Data

• Hazardous Substances Data: 851753-68-9(Hazardous Substances Data)

Upstream product

• 93249-44-6 2-fluoro-5-methylbenzaldehyde 
• 57260-71-6 1-t-Butoxycarbonylpiperazine 
• 24424-99-5 di-tert-butyl dicarbonate 

Downstream Products

• 869478-43-3 4-{4-methyl-2-[(S)-3-methyl-1-((S_S)-2-methyl-propane-2-sulfinylamino)-butyl]-phenyl}-piperazine-1-carboxylic acid tert-butyl ester 
• 869478-60-4 4-{4-methyl-2-[(S)-2-methyl-1-(2-methyl-propane-2-sulfonylamino)-propyl]-phenyl}-piperazine-1-carboxylic aicd tert-butyl ester 
• 851484-99-6 4-{4-methyl-2-[(S)-2-methyl-1-((S_S)-2-methyl-propane-2-sulfinylamino)-propyl]-phenyl}-piperazine-1-carboxylic acid tert-butyl ester 
• 869478-55-7 4-[2-((S)-1-amino-2-methyl-propyl)-4-methyl-phenyl]-piperazine-1-carboxylic acid tert-butyl ester 
• 869478-56-8 (S_S)-2-methyl-propane-2-sulfinic acid [(S)-2-methyl-1-(5-methyl-2-piperazin-1-yl-phenyl)-propyl]-amide 
• 869478-27-3 4-{4-methyl-2-[((S_S)-2-methyl-propane-2-sulfinylimino)-methyl]-phenyl}-piperazine-1-carboxylic acid tert-butyl ester 

Relevant articles and documents

Novel, versatile three-step synthesis of 1,2,3,4,10,10a-hexahydro- pyrazino[1,2- a ]indoles by intramolecular carbene-mediated C-H insertion

A new convenient three-step synthesis of the privileged CNS scaffold 1,2,3,4,10,10a-hexahydropyrazino[1,2-a]indoles has been developed. The method makes use of an intramolecular carbene-mediated C-H insertion in phenylpiperazine-derived tosyl-hydrazones m

Practical asymmetric synthesis of α-branched 2- piperazinylbenzylamines by 1,2-additions of organometallic reagents to N-tert-butanesulfinyl imines

2-[4-(tert-Butoxycarbonyl)piperazinyl] benzylidene-tert-butanesulfinamides underwent nucleophilic 1,2-addition with different organometallic reagents to give highly diastereomerically enriched adducts. X-ray crystallography of the resulting α-branched N-B