133981-12-1

Basic information

• Product Name: (S)-N-(1-Phenyleth-1-yl)-N-<(E)-hex-2-en-1-yl>-N'-tosylurea
• CAS NO: 133981-12-1
• Molecular Weight: 400.542
• Mol File: 133981-12-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-N-(1-Phenyleth-1-yl)-N-<(E)-hex-2-en-1-yl>-N'-tosylurea(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-N-(1-Phenyleth-1-yl)-N-<(E)-hex-2-en-1-yl>-N'-tosylurea(133981-12-1)
• EPA Substance Registry System: (S)-N-(1-Phenyleth-1-yl)-N-<(E)-hex-2-en-1-yl>-N'-tosylurea(133981-12-1)

Safety Data

• Hazardous Substances Data: 133981-12-1(Hazardous Substances Data)

Upstream product

• 99704-81-1 trans-2-hexenyl mesylate 
• 928-95-0 (E)-2-Hexen-1-ol 
• 4083-64-1 Tosyl isocyanate 
• 133981-08-5 (S)-N-(1-Phenyleth-1-yl)-N-<(E)-hex-2-en-1-yl>-amine 

Downstream Products

• 134003-72-8 (1'S,1''R,5R)-1-Tosyl-3-(1'-phenyleth-1'-yl)-5-(1''-iodoprop-1''-yl)-imidazolidin-2-one 
• 134003-70-6 (1'S,1''S,5S)-1-Tosyl-3-(1'-phenyleth-1'-yl)-5-(1''-iodoprop-1''-yl)-imidazolidin-2-one 

Relevant articles and documents

A new approach to the synthesis of enantiomerically pure 2,3-diaminoacids through chiral imidazolidin-2-ones

The synthesis of enantiomerically pure 5-iodomethylimidazolidin-2-ones (3a-c) and (4a-c) is reported, by means of iodocyclisation of allylic tosylureas (2a-c). Starting from pure (3a) and (4a), a synthesis of both (R)- and (S)-2,3-diaminopropanoic acid is