87791-00-2

Basic information

• Product Name: 2-Cyclohexen-1-one, 6-(1-hydroxy-1-methylethyl)-3-methyl-
• Synonyms: 2-Cyclohexen-1-one, 6-(1-hydroxy-1-methylethyl)-3-methyl-
• CAS NO: 87791-00-2
• Molecular Formula: C₁₀H₁₆O₂
• Molecular Weight: 0
• Mol File: 87791-00-2.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Cyclohexen-1-one, 6-(1-hydroxy-1-methylethyl)-3-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Cyclohexen-1-one, 6-(1-hydroxy-1-methylethyl)-3-methyl-(87791-00-2)
• EPA Substance Registry System: 2-Cyclohexen-1-one, 6-(1-hydroxy-1-methylethyl)-3-methyl-(87791-00-2)

Safety Data

• Hazardous Substances Data: 87791-00-2(Hazardous Substances Data)

Upstream product

• 98-55-5 terpineol 
• 89-82-7 pulegone 
• 54781-27-0 4-methyl-2-trimethylsilyloxycyclohexa-1,3-diene 
• 67-64-1 acetone 
• 75-65-0 tert-butyl alcohol 
• 71-43-2 benzene 
• 15910-72-2 cis-p-menth-2-ene-1,8-diol 
• 554-61-0 2-carene 

Downstream Products

• 6252-34-2 6-(1-hydroxy-1-methylethyl)-3-methyl-2-cyclohexen-1-ol 
• 119717-27-0 N-<(R)-1-phenylethyl>-O-<(3R,4S)-8-hydroxy-1-p-menthen-3-yl>urethane 
• 119614-28-7 N-<(R)-1-phenylethyl>-O-<(3S,4S)-8-hydroxy-1-p-menthen-3-yl>urethane 
• 119717-25-8 N-<(R)-1-phenylethyl>-O-<(3R,4R)-8-hydroxy-1-p-menthen-3-yl>urethane 
• 119717-26-9 N-<(R)-1-phenylethyl>-O-<(3S,4R)-8-hydroxy-1-p-menthen-3-yl>urethane 
• 119678-35-2 (3S,4S)-p-menth-1-ene-3,8-diol 
• 119678-38-5 (3R,4S)-1-p-menthene-3,8-diol 
• 71697-78-4 (3S,4R)-1-p-menthene-3,8-diol 
• 87859-10-7 (3R,4R)-p-menth-1-ene-3,8-diol 
• 71697-77-3 6β-(2'-hydroxyisopropyl)-3-methyl-2-cyclohexenone 
• 10482-56-1 (-)-(S)-α-terpineol 
• 3564-95-2 (1RS,3RS,4RS)-p-menthane-3,8-diol 
• 3564-95-2 (1RS,3SR,4RS)-p-menthane-3,8-diol 

Relevant articles and documents

PROCESS AND COMPOUNDS FOR PREPARATION OF CANNABINOIDS

The invention involves condensation of various derivatives of cyclic alkene alcohols of Formula (II) or Formula (III) where, R1 is alkyl, aryl, alkyl aryl or heterocyclic carbamoyl. R2 is either R1 as mentioned earlier or an acyl group, -C(=O)-R3 where, R3 is selected from a group comprising (subst)C1-C12 alkyl, (subst)aryl, alkyl aryl with olivetol to get (-)-trans-?9-tetrahydrocannabinol (also known as Dronabinol, Formula (I)). The process disclosed provides high purity of dronabinol at crude stage making it easy for purification.

Synthesis of Aristotelia-type alkaloids. Part III- (3R,4R)- and (3R,4S)-1-p-menthene-3,8-diol and the corresponding racemates: Preparation and assignment of configuration

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OXIDATION OF CARENE BY THALLIUM(III) ACETATE

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