910216-67-0

Basic information

• Product Name: tert-butyl N-(3-oxocylohex-1-enyl)-N-(prop-2-ynyl)carbamate
• Synonyms: tert-butyl N-(3-oxocylohex-1-enyl)-N-(prop-2-ynyl)carbamate
• CAS NO: 910216-67-0
• Molecular Weight: 249.31
• Mol File: 910216-67-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: tert-butyl N-(3-oxocylohex-1-enyl)-N-(prop-2-ynyl)carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl N-(3-oxocylohex-1-enyl)-N-(prop-2-ynyl)carbamate(910216-67-0)
• EPA Substance Registry System: tert-butyl N-(3-oxocylohex-1-enyl)-N-(prop-2-ynyl)carbamate(910216-67-0)

Safety Data

• Hazardous Substances Data: 910216-67-0(Hazardous Substances Data)

Upstream product

• 504-02-9 1,3-cylohexanedione 
• 24424-99-5 di-tert-butyl dicarbonate 
• 69042-21-3 (N-propargyl)-3-amino-2-cyclohexenone 

Downstream Products

• 910216-68-1 tert-butyl N-(buta-2,3-dienyl)-N-(3-oxocylohex-1-enyl)-carbamate 
• 910216-69-2 3-buta-2,3-dienylamino-cyclohex-2-enone 

Relevant articles and documents

Transition metal-free cyclization of N-boc-N-propargylenamines

An efficient method for the synthesis of multi-substituted pyrroles was developed using basic cyclization of readily accessible N-Boc-N-propargylenamines. Despite the basic conditions, cleavage of the N-Boc group occurred easily. The process was rapid and afforded N-H-pyrroles with wide functional group tolerance in high yields.

Intramolecular photoaddition of vinylogous amides with allenes: A novel approach to the synthesis of pyrroles

Irradiation of vinylogous amide or imide 5 (R = H, alkyl, or Ac) leads to the selective formation of either crossed photoadduct 7 (R = Ac) or parallel photoadduct 8 (R = H or alkyl) as a function of the nature of the group R. The latter result leads to a