1438279-61-8

Basic information

• Product Name: (S)-N-allyl-4-methyl-N-(1-(pentyloxy)allyl)benzenesulfonamide
• Synonyms: (S)-N-allyl-4-methyl-N-(1-(pentyloxy)allyl)benzenesulfonamide
• CAS NO: 1438279-61-8
• Molecular Weight: 337.483
• Mol File: 1438279-61-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (S)-N-allyl-4-methyl-N-(1-(pentyloxy)allyl)benzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-N-allyl-4-methyl-N-(1-(pentyloxy)allyl)benzenesulfonamide(1438279-61-8)
• EPA Substance Registry System: (S)-N-allyl-4-methyl-N-(1-(pentyloxy)allyl)benzenesulfonamide(1438279-61-8)

Safety Data

• Hazardous Substances Data: 1438279-61-8(Hazardous Substances Data)

Upstream product

• 50487-71-3 4-methyl-N-(2-propenyl)benzenesulfonamide 
• 166319-26-2 1-(propa-1,2-dien-1-yloxy)pentane 

Downstream Products

• 1438279-62-9 (S)-2-(pentyloxy)-1-tosyl-2,5-dihydro-1H-pyrrole 
• 1438279-73-2 (2S,3R,4R)-2-(pentyloxy)-1-tosylpyrrolidine-3,4-diol 

Relevant articles and documents

Access to trans-3,4-Dihydroxy-2-alkylpyrrolidines and piperidines by use of stereodefined cyclic N,O-Acetals as a Diversity-generating element

A highly efficient and stereoselective synthetic pathway towards trans-3,4-dihydroxy-2-alkylpyrrolidines and piperidines is described. The nature of the protecting groups on the hydroxyl moieties played a crucial role on the trans selectivity. By using this method, a concise total synthesis of (-)-2-epilentiginosine has been achieved.

Synthetic strategy for cyclic amines: A stereodefined cyclic N,O-acetal as a stereocontrol and diversity-generating element

In control: A new synthetic strategy towards cyclic amines was developed and exploits a stereodefined cyclic N,O-acetal as the key stereocontrol and diversity-generating element. The cyclic N,O-acetal was prepared from the sequential asymmetric hydroamina