123966-62-1

Basic information

• Product Name: (+/-)-3-allyl-2,4,4-trimethyl-cyclohexanone
• Synonyms: (+/-)-3-allyl-2,4,4-trimethyl-cyclohexanone
• CAS NO: 123966-62-1
• Molecular Weight: 180.29
• Mol File: 123966-62-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (+/-)-3-allyl-2,4,4-trimethyl-cyclohexanone(CAS DataBase Reference)
• NIST Chemistry Reference: (+/-)-3-allyl-2,4,4-trimethyl-cyclohexanone(123966-62-1)
• EPA Substance Registry System: (+/-)-3-allyl-2,4,4-trimethyl-cyclohexanone(123966-62-1)

Safety Data

• Hazardous Substances Data: 123966-62-1(Hazardous Substances Data)

Upstream product

• 1629-58-9 4-penten-3-one 
• 13395-71-6 2,4,4-trimethyl-2-cyclohexenone 
• 762-72-1 allyl-trimethyl-silane 

Downstream Products

• 132751-19-0 6(S*)-(methoxymethoxy)-3(R*),8,8-trimethylbicyclo<2.2.2>octan-2-one tosylhydrazone 
• 116428-67-2 ((S)-2,2,6-Trimethyl-5-oxo-cyclohexyl)-acetic acid 

Relevant articles and documents

LIMITATIONS IN THE APPLICATION OF ANIONIC OXY-COPE SIGMATROPY TO ELABORATION OF THE FORSKOLIN NUCLEUS

The functionalized bicyclooctenone 6 has been synthesized in four steps from 2,4,4-trimethyl-2-cyclohexenone.This ketone undergoes 1,2-addition with 6-lithiodihydropyran to deliver alcohols 16 and 17 in a 1:1.8 ratio.The potassium salt of 17 experi

SYNTHESIS OF THE FORSKOLIN SKELETON VIA ANIONIC OXY-COPE REARRANGEMENT

The forskolin prototype 14 has been elaborated in 9 steps from 2,4,4-trimethyl-cyclohexenone (5), the entire ring system materializing during oxyanionic Cope rearrangement of alcohol 10.