1399008-27-5

Basic information

• Product Name: N,N'-(2S,2'S)-2,2'-(2-iodo-1,3-phenylene)bis(oxy)bis(propane-2,1-diyl)bis(2,4,6-trimethylbenzamide)
• Synonyms: N,N'-(2S,2'S)-2,2'-(2-iodo-1,3-phenylene)bis(oxy)bis(propane-2,1-diyl)bis(2,4,6-trimethylbenzamide)
• CAS NO: 1399008-27-5
• Molecular Weight: 642.577
• Mol File: 1399008-27-5.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 691.0±55.0 °C(Predicted)
• Density: 1.302±0.06 g/cm3(Predicted)
• CAS DataBase Reference: N,N'-(2S,2'S)-2,2'-(2-iodo-1,3-phenylene)bis(oxy)bis(propane-2,1-diyl)bis(2,4,6-trimethylbenzamide)(CAS DataBase Reference)
• NIST Chemistry Reference: N,N'-(2S,2'S)-2,2'-(2-iodo-1,3-phenylene)bis(oxy)bis(propane-2,1-diyl)bis(2,4,6-trimethylbenzamide)(1399008-27-5)
• EPA Substance Registry System: N,N'-(2S,2'S)-2,2'-(2-iodo-1,3-phenylene)bis(oxy)bis(propane-2,1-diyl)bis(2,4,6-trimethylbenzamide)(1399008-27-5)

Safety Data

• Hazardous Substances Data: 1399008-27-5(Hazardous Substances Data)

Upstream product

• 1399008-15-1 (2S,2'S)-2,2'-((2-iodo-1,3-phenylene)bis(oxy))bis(propan-1-amine) 
• 938-18-1 mesitylene-2-carboxylic acid chloride 
• 1399008-14-0 di-tert-butyl ((2S,2'S)-((2-iodo-1,3-phenylene)bis(oxy))bis(propane-2,1-diyl))dicarbamate 
• 41046-67-7 2-iodoresorcinol 
• 1452925-79-9 C₃₄H₄₁IN₂O₈ 
• 885025-51-4 3-(3,5-di-tert-butyl-2-hydroxyphenyl)propanoic acid 
• 1399009-21-2 C₃₆H₄₅IN₂O₈ 

Downstream Products

• 1452925-32-4 N,N'-((2S,2'S)-((2-iodo-1,3-phenylene)bis(oxy))bis(propane-2,1-diyl))bis(N,2,4,6-tetramethylbenzamide) 
• 1399009-21-2 C₃₆H₄₅IN₂O₈ 
• 1452925-38-0 C₃₄H₄₅IN₂O₆ 
• 1452925-78-8 C₃₄H₃₅⁽²⁾H₆IN₂O₈ 
• 1452925-77-7 C₃₆H₃₉⁽²⁾H₆IN₂O₈ 

Relevant articles and documents

Synthesis of chiral organoiodine catalyst for enantioselective oxidative dearomatization reactions: N,n'-(2s,2's)-(2-iodo-1,3-phenylene)bis(oxy)bis(propane-2,1-diyl)bis(2,4,6-trimethylbenzamide)

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Hydrogen bonding and alcohol effects in asymmetric hypervalent iodine catalysis: Enantioselective oxidative dearomatization of phenols

Iodine chooses: A conformationally flexible C2-symmetric organoiodine(III) catalyst for the highly enantioselective catalytic oxidative dearomatization of phenols has been developed. Catalysis is controlled by intramolecular hydrogen-bonding interactions and additional achiral alcohols. Copyright