75347-10-3

Upstream product

• 22818-69-5 (3-nitropropyl)benzene 
• 1197-50-8 (Z)-3-phenylpropionaldehyde oxime 
• 75336-73-1 1-chloro-3-phenylpropanal oxime 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 104-53-0 3-phenyl-propionaldehyde 
• 1197-50-8 3-phenylpropanal oxime 
• 92988-96-0 N-hydroxy(2-phenylethyl)-oximidoyl chloride 
• 40591-65-9 2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl isothiouronium bromide 
• 637-59-2 1-Bromo-3-phenylpropane 
• 19879-84-6 tetraacetyl thioglucose 
• 75336-75-3 S-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-3-phenylpropanothiohydroximate 

Downstream Products

• 18425-76-8 2-phenethylglucosinolate 

Relevant academic research and scientific papers

Synthesis and anti-inflammatory activity of aromatic glucosinolates

Aromatic GLs are important members of the glucosinolate family of compounds because of their potential biological activity and medicinal properties. This study has shown success in the high yielding synthesis of some important aromatic GLs as well as the results of testing for anti-inflammatory properties of the synthetic GLs. 3,4-Dimethoxyphenylglucosinolate was found to be the most active anti-inflammatory of the seven glucosinolates assayed.

Analysis of intact glucosinolates by MALDI-TOF mass spectrometry.

Glucosinolates are naturally occurring plant compounds that may be important in the dietary prevention of cancer. This study shows that they can be detected in their intact form by matrix-assisted laser desorption/ionization time-of-flight mass spectromet

Synthesis of glucosinolates

A high yielding synthesis of 2-phenethylglucosinolate is described. The method should also be directly applicable to most (if not all) other glucosinolates.