274682-99-4

Upstream product

• 1076-43-3 benzene-d6 
• 19547-01-4 1,2,2,2-tetradeuterio-1-(2,3,4,5,6-pentadeuteriophenyl)ethanol 
• 19547-00-3 <2H8>Acetophenone 
• 28077-64-7 acetophenone-d5 
• 68239-29-2 (+/-)-1-phenylethyl bromide-d9 

Downstream Products

• 357407-81-9 (1S)-α-methylbenzylamine-d9 
• 274682-96-1 (R)-α-methylbenzylamine 
• 357407-84-2 C₁₁⁽²⁾H₁₂F₃NO 
• 357407-83-1 (1S)-N-trifluoroacetyl-α-methylbenzylamine-d9 
• 357407-86-4 (1R)-N,α-dimethylbenzylamine-d13 
• 357407-86-4 (1S)-N,α-dimethylbenzylamine-d13 

Relevant academic research and scientific papers

Direct observation of deuterium migration in crystalline-state reaction by single-crystal neutron diffraction. II. 3-1 photoisomerization of a cobaloxime complex

Single crystal neutron diffraction analysis of photo-exposed (3-cyanopropyl-d2 α,α)-[(R)-1-phenylethylamine-d 11]bis(dimethylglyoximato-d14)cobalt(III) was carried out in order to clarify the mechanism of the cr

Toward the creation of NMR databases in chiral solvents for assignments of relative and absolute stereochemistry: proof of concept.

[structure: see text] An NMR database approach in a chiral solvent allows us to predict both relative and absolute stereochemistry of an unknown compound without degradation and/or derivatization. N,alpha-Dimethylbenzylamine (DMBA) is a suitable solvent for this purpose. Using the C.5-C.10 portion of oasomycin A, the feasibility and reliability of this approach is demonstrated.