100572-83-6

Basic information

• Product Name: 4-(1,5-dimethyl-4-hexenyl)-3-cyclohexen-1-one
• Synonyms: 4-(1,5-dimethyl-4-hexenyl)-3-cyclohexen-1-one
• CAS NO: 100572-83-6
• Molecular Weight: 206.328
• Mol File: 100572-83-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4-(1,5-dimethyl-4-hexenyl)-3-cyclohexen-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(1,5-dimethyl-4-hexenyl)-3-cyclohexen-1-one(100572-83-6)
• EPA Substance Registry System: 4-(1,5-dimethyl-4-hexenyl)-3-cyclohexen-1-one(100572-83-6)

Safety Data

• Hazardous Substances Data: 100572-83-6(Hazardous Substances Data)

Upstream product

• 68178-48-3 2-(4-Methoxyphenyl)-6-methyl-5-hepten-2-ol 
• 110-93-0 6-Methyl-hept-5-en-2-on 
• 81841-89-6 4,4-(ethylenedioxy)-1-(phenylsulfonyl)cyclohexene 
• 4582-61-0 2-<(tolylsulfonyl)oxy>-6-methyl-5-heptene 
• 78-94-4 methyl vinyl ketone 
• 344903-14-6 8-Benzenesulfonyl-8-(1,5-dimethyl-hex-4-enyl)-1,4-dioxa-spiro[4.5]dec-6-ene 
• 100572-82-5 1-(1,5-dimethyl-4-hexenyl)-4-methoxy-1,4-cyclohexadiene 
• 100572-91-6 (E,Z)-4-(1,5-Dimethyl-1,4-hexadienyl)-1-methoxybenzol 

Downstream Products

• 1723-81-5 (1R,4R)-1-methyl-4-(6-methylhept-5-en-2-yl)cyclohex-2-enol 
• 1723-81-5 (1S,4R)-4-(1,5-Dimethyl-hex-4-enyl)-1-methyl-cyclohex-2-enol 
• 644-30-4 ar-curcumene 
• 451-55-8 γ-curcumene 
• 72345-84-7 (+/-)-β-curcumene 
• 1723-80-4 4-(6-methyl-5-hepten-2-yl)-2-cyclohexen-1-one 
• 139623-49-7 4-(1,5-Dimethyl-4-hexenyl)-1-methyl-3-cyclohexen-1-ol 

Relevant articles and documents

4-alkenyl-1-methoxy-1,4-cyclohexadienes by tandem addition-multistep reduction of alkenyl aldehydes and ketones. Synthesis of 4-alkenyl-3-cyclohexen-1-ones by subsequent hydrolysis

A series of 4-alkenyl-1-methoxy-1,4-cyclohexadienes were prepared by a tandem addition-multistep reduction procedure. This one-pot process included the addition of 4-methoxyphenyllithium to alkenyl aldehydes and ketones, followed by multistep reduction of

Efficient Syntheses of β-Sesquiphellandrene and Zingiberenol Employing a Tandem Arylation-Multistep Reduction-Hydrolysis Sequence

The title sesquiterpenes are synthesized in one step from the common intermediate 4-(6-methyl-5-hepten-2-yl)-2-cyclohexen-1-one, which is prepared using a one-pot tandem arylation-multistep reduction-hydrolysis sequence.

Intramolecular Photoaddition of a 1,7-Diene

Intramolecular photoaddition of the 1,7-diene system in 4-(1,5-dimethylhex-4-enyl)cyclohex-2-enone (3) yielded, inter alia, two ketones containing the tricyclo5,11>undecan-8-one system.The structure and stereochemistry of these ketones has been determined from X-ray crystallographic analyses of suitable derivatives.