29474-11-1

Basic information

• Product Name: 1-Cyclohexene-1-methanol, 2-methyl-
• Synonyms: 1-Hydroxymethyl-2-methyl-1-cyclohexene;1-Cyclohexene-1-methanol,2-methyl
• CAS NO: 29474-11-1
• Molecular Formula: C8H14O
• Molecular Weight: 126.199
• Mol File: 29474-11-1.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 100-104 °C(Press: 12 Torr)
• Density: 0.939±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1-Cyclohexene-1-methanol, 2-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Cyclohexene-1-methanol, 2-methyl-(29474-11-1)
• EPA Substance Registry System: 1-Cyclohexene-1-methanol, 2-methyl-(29474-11-1)

Safety Data

• Hazardous Substances Data: 29474-11-1(Hazardous Substances Data)

Upstream product

• 1655-07-8 ethyl 2-oxocyclohexane carboxylate 
• 122135-83-5 ethyl 2-trifluoromethanesulfonyloxycyclohex-1-enecarboxylate 
• 25662-38-8 2-methyl-1-cyclohexenecarboxylic acid methyl ester 
• 71712-64-6 2-(Diethoxy-phosphoryloxy)-cyclohex-1-enecarboxylic acid methyl ester 
• 41302-34-5 2-(methoxycarbonyl)cyclohexanone 
• 104654-69-5 Ethyl 2-methyl-1-cyclohex-1-ene carboxylate 
• 50-00-0 formaldehyd 
• 591-49-1 1-methylcyclohex-1-ene 
• 75-24-1 trimethylaluminum 
• 54625-15-9 2-methylcyclohex-1-ene-1-carbaldehyde 

Downstream Products

• 52329-96-1 1-methyl-2-((phenylcarbonyl)methyl)-1-cyclohexene 
• 63704-29-0 1,2-bis-(2-methyl-cyclohex-1-enyl)-ethane 
• 432555-17-4 (R)-(2-methyl-1-cyclohexenyl)(methyldiphenylsilyl)methyl N,N-diisopropylcarbamate 
• 804566-50-5 {1Z,1[2S,2(1R)]}-{2-[1-(4-bromophenyl)-1-hydroxymethyl]methylcyclohexylidene}methyl N,N-diisopropylcarbamate 
• 432555-18-5 (R)-(2-methyl-1-cyclohexenyl)(methyldiphenylsilyl)methanol 
• 432555-24-3 (2-methyl-1-cyclohexenyl)methyl N,N-diisopropylcarbamate 
• 2819-48-9 1,2-bis(methylene)cyclohexane 

Relevant articles and documents

PhI(OAc)2-mediated alkoxyoxygenation of β,γ-unsaturated ketoximes: Preparation of isoxazolines bearing two contiguous tetrasubstituted carbons

A PhI(OAc)2-promoted dioxygenation of allyl oximes, including one alkoxylation, has been developed. This reaction can give isoxazoline products bearing two contiguous tetrasubstituted carbons. Various oximes substrates bearing different aryl groups and tetrasubstituted-olefin moieties were compatible with the mild reaction conditions. A two-electron oxidation pathway was proposed based on results of preliminary mechanistic studies.

SUBSTITUTED QUINOLIZINE DERIVATIVES USEFUL AS HIV INTEGRASE INHIBITORS

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Intramolecular additions of allylsilanes to conjugated dienones. A direct stereoselective synthesis of (±)-14-deoxyisoamijiol

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