113489-32-0

Basic information

• Product Name: 3-Cyclohexene-1-carboxamide, N-methoxy-N-methyl-
• CAS NO: 113489-32-0
• Molecular Formula: C9H15NO2
• Molecular Weight: 169.224
• Mol File: 113489-32-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-Cyclohexene-1-carboxamide, N-methoxy-N-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Cyclohexene-1-carboxamide, N-methoxy-N-methyl-(113489-32-0)
• EPA Substance Registry System: 3-Cyclohexene-1-carboxamide, N-methoxy-N-methyl-(113489-32-0)

Safety Data

• Hazardous Substances Data: 113489-32-0(Hazardous Substances Data)

Upstream product

• 4771-80-6 1,2,5,6-tetrahydrobenzoic acid 
• 1117-97-1 N,0-dimethylhydroxylamine 
• 6638-79-5 N,O-dimethylhydroxylamine*hydrochloride 

Downstream Products

• 17382-40-0 1-Cyclohex-3-enyl-hept-2-yn-1-one 
• 661467-31-8 3-[1-(3-cyclohex-3-enyl-3(R,S)-hydroxypropyl)-3(R),4(R)-dimethylpiperidin-4-yl]phenol 
• 661467-30-7 1-Cyclohex-3-enyl-3-[(3R,4R)-4-(3-hydroxy-phenyl)-3,4-dimethyl-piperidin-1-yl]-propan-1-one 
• 1383688-35-4 4'-fluoro-N-methoxy-N-methyl-2,3,4,5-tetrahydro-[1,1'-biphenyl]-4-carboxamide 
• 1383688-36-5 4'-chloro-N-methoxy-N-methyl-2,3,4,5-tetrahydro-[1,1'-biphenyl]-4-carboxamide 
• 1383688-37-6 ethyl-4'-(methoxy(methyl)carbamoyl)-2',3',4',5'-tetrahydro-[1,1'-biphenyl]-4-carboxylate 
• 1383688-38-7 N-methoxy-N-methyl-4'-nitro-2,3,4,5-tetrahydro-[1,1'-biphenyl]-4-carboxamide 
• 1383688-39-8 3'-bromo-N-methoxy-N-methyl-2,3,4,5-tetrahydro-[1,1'-biphenyl]-4-carboxamide 
• 1383688-40-1 N-methoxy-N-methyl-3'-(trifluoromethyl)-2,3,4,5-tetrahydro-[1,1'-biphenyl]-4-carboxamide 
• 1383688-42-3 4-(6-fluoropyridin-3-yl)-N-methoxy-N-methylcyclohex-3-enecarboxamide 
• 1383688-32-1 N-methoxy-N-methyl-2,3,4,5-tetrahydro-[1,1'-biphenyl]-4-carboxamide 
• 1009-14-9 phenyl butyl ketone 
• 119-61-9 benzophenone 
• 831-14-1 cyclohex-3-en-1-yl(phenyl)methanone 

Relevant articles and documents

A new strategy for accessing (S)-1-(furan-2-yl)pent-4-en-1-ol: a key precursor of Ipomoeassin family of compounds and C1–C15 domain of halichondrins

A highly efficient synthesis of (S)-1-(furan-2-yl)pent-4-en-1-ol, known to be an initial precursor of Ipomoeassin family of compounds and C1–C15 domain of halichondrins has been achieved via a sequence involving the use of Weinreb amide formation followed by Weinreb ketone synthesis and finally CBS (Corey–Bakshi–Shibata) reduction. Detailed study on improvement of each step is described. The title compound was converted to a potential cytotoxic agent for further pharmacological studies.

Na+-dependent high affinity binding of [3H]LY515300, a 3,4-dimethyl-4-(3-hydroxyphenyl)piperidine opioid receptor inverse agonist

Analogues of 3,4-dimethyl-4-(3-hydroxyphenyl)piperidines are high affinity inverse agonists for μ-, δ- and κ-opioid receptors. To characterize inverse agonist binding, we synthesized a high specific activity radioligand from this series, [3H]LY