130740-96-4

Basic information

• Product Name: 1-(2,6,6-trimethyl-cyclohex-1-enyl)-but-3-yn-1-ol
• Synonyms: 1-(2,6,6-trimethyl-cyclohex-1-enyl)-but-3-yn-1-ol
• CAS NO: 130740-96-4
• Molecular Weight: 192.301
• Mol File: 130740-96-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-(2,6,6-trimethyl-cyclohex-1-enyl)-but-3-yn-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2,6,6-trimethyl-cyclohex-1-enyl)-but-3-yn-1-ol(130740-96-4)
• EPA Substance Registry System: 1-(2,6,6-trimethyl-cyclohex-1-enyl)-but-3-yn-1-ol(130740-96-4)

Safety Data

• Hazardous Substances Data: 130740-96-4(Hazardous Substances Data)

Upstream product

• 432-25-7 2,6,6-trimethylcyclohex-1-enecarbaldehyde 
• 106-96-7 propargyl bromide 
• 18295-60-8 propargyl magnesium bromide 

Downstream Products

• 130740-97-5 tert-Butyl-dimethyl-[1-(2,6,6-trimethyl-cyclohex-1-enyl)-but-3-ynyloxy]-silane 

Relevant articles and documents

Efficient propargylation of aldehydes and ketones catalyzed by titanocene(III)

We describe a novel method for the propargylation of a wide range of aldehydes and ketones catalyzed by titanocene(III) complexes under mild reaction conditions and compatible with many functional groups. Homopropargylic alcohols are obtained as the sole products even when ketones are used as starting materials, which is unusual in Barbier-type propargylations.

A synthesis of the abietane diterpenoid quinone (±)-royleanone via maleoylcobalt technology

(±)-Royleanone has been synthesized by rapid construction of a highly substituted quinone using maleoylcobalt complex technology followed by acid induced cyclization of the corresponding hydroquinone methyl ether onto a tethered enone. The synthesis was completed by straightforward functional group manipulations.