105866-12-4

Basic information

• Product Name: 1-Nonanol, 9-(phenylsulfonyl)-
• CAS NO: 105866-12-4
• Molecular Formula: C15H24O3S
• Molecular Weight: 284.42
• Mol File: 105866-12-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-Nonanol, 9-(phenylsulfonyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Nonanol, 9-(phenylsulfonyl)-(105866-12-4)
• EPA Substance Registry System: 1-Nonanol, 9-(phenylsulfonyl)-(105866-12-4)

Safety Data

• Hazardous Substances Data: 105866-12-4(Hazardous Substances Data)

Upstream product

• 50816-19-8 8-bromooctanol 
• 3112-85-4 methylphenylsulfonate 
• 55362-80-6 9-bromononan-1-ol 
• 873-55-2 sodium benzenesulfonate 
• 51308-99-7 9-chloro-1-nonanol 

Downstream Products

• 884843-02-1 9-(benzenesulfonyl)nonanal 
• 105866-20-4 Acetic acid (E)-9-benzenesulfonyl-tetradec-9-enyl ester 
• 105866-19-1 Acetic acid (E)-9-benzenesulfonyl-dodec-9-enyl ester 
• 105866-18-0 Phenylsulfonyl-9 tetradecene-9E ol-1 
• 105866-17-9 Phenylsulfonyl-9 dodecene-9E ol-1 
• 16974-11-1 (Z)-9-dodecenyl acetate 
• 16725-53-4 (Z)-9-tetradecen-1-yl acetate 
• 35153-15-2 (Z)-9-tetradecen-1-ol 
• 871334-79-1 6-benzenesulfonyl-14-(tert-butyl-dimethyl-silanyloxy)-2-hydroxy-tetradecan-5-one 
• 884843-04-3 (5Z,25Z)-17-benzenesulfonyl-5,25-hentriacontadiene 
• 884843-03-2 (Z)-15-benzenesulfonyl-6-pentadecene 
• 871334-78-0 (9-benzenesulfonyl-nonyloxy)-tert-butyl-dimethyl-silane 

Relevant articles and documents

A synthetic approach to sporotricale methylether

A synthetic approach to sporotricale methylether, a metabolite of the fungus Sporotrichum laxum with inhibitory activity against Helicobacter pylori, is described. The synthesis relies on the condensation of 13-hydroxy-10- oxotetradecanal, prepared via reaction of a sulfone-activated moiety with valerolactone, with diethyl 3,5-dimethoxyphthalide-7-phosphonate. Georg Thieme Verlag Stuttgart.

SYNTHESES A L'AIDE DE SULFONES (XXXVII). SYNTHESE DE TROIS PHEROMONES A UNE DOUBLE LIAISON Z : Z, 8-DDA; Z, 9-DDA; Z, 9-TDA.

The title compounds Z,8-dodecen-1yl acetate, Z,9-dodecen-1yl acetate and Z,9-tetradecen-1yl-acetate have been synthesized in three efficient steps: the reaction mixture from metalated ω-hydroxy sulfones and appropriate aldehydes was quenched with acetic anhydride yielding a diastereoisomeric mixture of β-acetoxy sulfones.Convergent elimination with powdered sodium hydroxide led to the E vinylic sulfone.Stereospecific hydrogenolysis of the sulfonyl group was carried out with sodium dithionite leading to the unsaturated alcohol (> 99percent Z).