1173373-69-7

Basic information

• Product Name: N-[(1S,2S)-2-(diMethylaMino)cyclohexyl]-N'-[[(1R,4aS,10aR)-1,2,3,4,4a,9,10,10a-octahydro-1,4a-diMethyl-7-(1-Methylethyl)-1-phenanthrenyl]Methyl]-Thiourea
• Synonyms: N-[(1S,2S)-2-(diMethylaMino)cyclohexyl]-N'-[[(1R,4aS,10aR)-1,2,3,4,4a,9,10,10a-octahydro-1,4a-diMethyl-7-(1-Methylethyl)-1-phenanthrenyl]Methyl]-Thiourea;N-[(1S,2S)-2-(Dimethylamino)cyclohexyl]-N'-[[(1R,4aS, 10aR)-1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7- isopropyl-1-phenanthrenyl]methyl]thiourea
• CAS NO: 1173373-69-7
• Molecular Formula: C₂₉H₄₇N₃S
• Molecular Weight: 469.76858
• Mol File: 1173373-69-7.mol
• Article Data: 1

Chemical Properties

• Melting Point: 82 °C
• Boiling Point: 557.0±60.0 °C(Predicted)
• Appearance: /
• Density: 1.07±0.1 g/cm3(Predicted)
• PKA: 13.80±0.40(Predicted)
• CAS DataBase Reference: N-[(1S,2S)-2-(diMethylaMino)cyclohexyl]-N'-[[(1R,4aS,10aR)-1,2,3,4,4a,9,10,10a-octahydro-1,4a-diMethyl-7-(1-Methylethyl)-1-phenanthrenyl]Methyl]-Thiourea(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(1S,2S)-2-(diMethylaMino)cyclohexyl]-N'-[[(1R,4aS,10aR)-1,2,3,4,4a,9,10,10a-octahydro-1,4a-diMethyl-7-(1-Methylethyl)-1-phenanthrenyl]Methyl]-Thiourea(1173373-69-7)
• EPA Substance Registry System: N-[(1S,2S)-2-(diMethylaMino)cyclohexyl]-N'-[[(1R,4aS,10aR)-1,2,3,4,4a,9,10,10a-octahydro-1,4a-diMethyl-7-(1-Methylethyl)-1-phenanthrenyl]Methyl]-Thiourea(1173373-69-7)

Safety Data

• Hazardous Substances Data: 1173373-69-7(Hazardous Substances Data)

Upstream product

• 115269-93-7 (1R,4aS)-7-isopropyl-1-(isothiocyanatomethyl)-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene 
• 67198-21-4 (±)-N,N-dimethyl-trans-1,2-diaminocyclohexane 

Relevant articles and documents

Enantio- and diastereoselective asymmetric addition of 1,3-dicarbonyl compounds to nitroalkenes in a doubly stereocontrolled manner catalyzed by bifunctional rosin-derived amine thiourea catalysts

(Chemical Equation Presented) Starting from commercially available natural rosin derivatives, a class of bifunctional rosin-derived amine thiourea catalysts were designed and synthesized. The doubly stereocontrolled asymmetric addition of a variety of 1,3