91230-88-5

Upstream product

• 4227-95-6 [13C]methyl iodide 
• 100-52-7 benzaldehyde 

Downstream Products

• 71777-36-1 acetophenone-β-¹³C 
• 158507-69-8 ethylbenzene 8-13C 
• 91230-93-2 (1S,2S,3R)-(+)-2-phenylcyclopropanecarboxylic-3-13C-1,2,3-2H₃ acid 
• 91230-87-4 (1R,2S,3R)-phenylcyclopropane-2-13C-1,2,3-2H₃ 
• 91230-94-3 (1S,2S,3R)-2-phenylcyclopropanemethanol-3-13C-1,2,3-2H₃ 
• 91230-89-6 phenylacetylene-2-13C-2-2H 
• 91230-91-0 styrene-β-13C-α,β-trans-2H2 
• 54522-92-8 phenylacetylene-2-13C 
• 946075-60-1 C₂₄⁽¹³⁾CH₃₃N 
• 946075-65-6 C₁₃⁽¹³⁾CH₁₈ 

Relevant academic research and scientific papers

Thermal Stereomutations of (2R,3R)-Phenylcyclopropane-1,2,3-2H3 and (1R,2S,3R)-Phenylcyclopropane-2-13C-1,2,3-2H3: Quantification of All Four Stereochemical Modes for Interconversions among the 1-Phenyl-1,2,3-trideuterocyclopropanes

Optically pure (2R,3R)-phenylcyclopropane-1,2,3-2H3 and (1R,2S,3R)-phenylcyclopropane-2-13C-1,2,3-2H3 have been prepared and the thermal stereomutations they exhibit have been followed kinetically at 309.3 deg C to provide the first complete quantificatio

Rearrangement of indene skeletons under mild conditions

(Chemical Equation Presented) Isomerization between two isomers of 1,2-disubstituted 3-aminoindenes occurs via the rearrangement of indene frameworks. In contrast to previous rearrangements of indene derivatives, which occur under high-temperature conditi

The carbonyl group as a reluctant transmitter of hyperconjugative or ?-? spin-spin coupling interactions in derivatives of benzaldehyde, acetophenone, and benzophenone

Unlike their counterparts in anisole or toluene derivatives, the six-bond spin-spin coupling constants bentween para ring protons or (19)F nuclei and protons or (13)C nuclei in the sidechain of derivatives of benzaldehyde, acetophenone, and benzophenone c