884845-78-7

Basic information

• Product Name: N-benzyl-N-methoxy-3-(2,6,6-trimethyl-cyclohex-1-enyl)-acrylamide
• Synonyms: N-benzyl-N-methoxy-3-(2,6,6-trimethyl-cyclohex-1-enyl)-acrylamide
• CAS NO: 884845-78-7
• Molecular Weight: 313.44
• Mol File: 884845-78-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-benzyl-N-methoxy-3-(2,6,6-trimethyl-cyclohex-1-enyl)-acrylamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-N-methoxy-3-(2,6,6-trimethyl-cyclohex-1-enyl)-acrylamide(884845-78-7)
• EPA Substance Registry System: N-benzyl-N-methoxy-3-(2,6,6-trimethyl-cyclohex-1-enyl)-acrylamide(884845-78-7)

Safety Data

• Hazardous Substances Data: 884845-78-7(Hazardous Substances Data)

Upstream product

• 20056-98-8 N-benzyl-N-methoxyamine 
• 884845-74-3 [(benzyl-methoxy-carbamoyl)-methyl]-phosphonic acid diethyl ester 
• 884845-72-1 N-benzyl-2-chloro-N-methoxy-acetamide 
• 884845-76-5 N-benzyl-N-methoxy-acrylamide 
• 99747-72-5 2,6,6-trimethylcyclohex-1-en-1-yl trifluoromethanesulfonate 

Downstream Products

• 210700-51-9 ((2E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-enyl)nona-2,6,8-trien-4-ynyloxy)(tert-butyl)dimethylsilane 
• 68-26-8 vitamine A 
• 37384-77-3 ethyl β-ionylidene acetate 
• 3917-40-6 (2Z,4E)-3-methyl-5-(2,6,6-trimethylcyclohex-1-enyl)penta-2,4-dienol 
• 25576-25-4 (3E,5E)-4-methyl-6-(2,6,6-trimethyl-1-cyclohexen-1-yl)-3,5-hexadien-1-yne 
• 29443-88-7 (2E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethyl-cyclohex-1-enyl)-nona-2,6,8-trien-4-yn-1-ol 
• 3917-39-3 (2E,4E)-3-methyl-5-(2,6,6-trimethyl-1-cyclohexenyl)-2,4-pentadien-1-ol 
• 3917-41-7 (2E,4E)-3-methyl-5-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4-pentadienal 
• 885050-34-0 [9,10-13C₂]-11Z-retinol 
• 79-77-6 (E)-β-ionone 

Relevant articles and documents

Accurate measurements of 13C-13C J-couplings in the rhodopsin chromophore by double-quantum solid-state NMR spectroscopy

A new double-quantum solid-state NMR pulse sequence is presented and used to measure one-bond 13C-13C J-couplings in a set of 13C2-labeled rhodopsin isotopomers. The measured J-couplings reveal a perturbation of the electronic structure at the terminus of the conjugated chain but show no evidence for protein-induced electronic perturbation near the C11-C12 isomerization site. This work establishes NMR methodology for measuring accurate 1JCC values in noncrystalline macromolecules and shows that the measured J-couplings may reveal local electronic perturbations of mechanistic significance. Copyright