74352-11-7

Upstream product

• 79-77-6 (E)-β-ionone 
• 106-96-7 propargyl bromide 
• 18295-60-8 propargyl magnesium bromide 

Downstream Products

• 74352-12-8 9-(2-propynyl)-β-ionyl acetate 
• 103169-93-3 3,8-dimethyl-1,10-bis-(2,6,6-trimethyl-cyclohex-1-enyl)-deca-1,3,7,9-tetraen-5-yne 
• 74352-09-3 11,12-dideuterio-all-trans-retinal 
• 74430-64-1 11,12-dideuterio-13-cis-retinal 
• 74410-14-3 11-cis-11,12-dideuteroretinal 
• 74352-09-3 C₂₀H₂₆⁽²⁾H₂O 
• 74352-13-9 (6E,8E)-1,1-Dimethoxy-3,7-dimethyl-9-(2,6,6-trimethyl-cyclohex-1-enyl)-nona-6,8-dien-4-yn-3-ol 
• 103633-89-2 3-(β-ionilidene)-1-propyne 
• 25576-25-4 (3E,5E)-4-methyl-6-(2,6,6-trimethyl-1-cyclohexen-1-yl)-3,5-hexadien-1-yne 
• 25576-26-5 (3Z,5E)-4-methyl-6-(2,6,6-trimethyl-1-cyclohexen-1-yl)-3,5-hexadien-1-yne 
• 7488-99-5 alpha-carotene 
• 472-89-9 ε-carotene 

Relevant academic research and scientific papers

A synthesis of oxolenes and furans via oxacyclopentylidene chromium and molybdenum complexes

An easy and convenient preparation of substituted oxolenes and furans by metal-assisted cyclization of alkynols using labile pentacarbonylchromium and pentacarbonylmolybdenum complexes is described.

10-Mono-, 11-mono-, 12-mono and 11,12-dideuteroretinal

The 11-mono and 12-mono- and 11,12-dideuteroretinal (in the all-trans, 9-cis, 11-cis and 13-cis form) with > 98percent chemical purity and > 95percent mono- and dideuterium incorporation were prepared using the same scheme for all three compounds.The all-