83421-78-7

Basic information

• Product Name: 2-Propenoyl azide, 3-(4-chlorophenyl)-, (2E)-
• CAS NO: 83421-78-7
• Molecular Formula: C9H6ClN3O
• Molecular Weight: 207.619
• Mol File: 83421-78-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-Propenoyl azide, 3-(4-chlorophenyl)-, (2E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenoyl azide, 3-(4-chlorophenyl)-, (2E)-(83421-78-7)
• EPA Substance Registry System: 2-Propenoyl azide, 3-(4-chlorophenyl)-, (2E)-(83421-78-7)

Safety Data

• Hazardous Substances Data: 83421-78-7(Hazardous Substances Data)

Upstream product

• 35086-79-4 cinnamoyl chloride 
• 104-88-1 4-chlorobenzaldehyde 

Downstream Products

• 24188-74-7 7-chloroisoquinoline-1(2Η)-one 
• 1616404-19-3 3-acetyl-4-hydroxy-5-(4-chlorophenyl)pyridin-2(1H)-one 
• 1616404-18-2 ethyl (E)-2-(((E)-4-chlorostyryl)carbamoyl)-3-hydroxybut-2-enoate 
• 1616404-15-9 ethyl 4-hydroxy-5-(4-chlorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylate 
• 1616404-13-7 (E)-4-hydroxy-5-(4-chlorophenyl)-N-(4-chlorostyryl)-2-oxo-1,2-dihydropyridine-3-carboxamide 
• 1616404-09-1 C₁₆H₁₈ClNO₅ 
• 78974-23-9 Sodium; (2S,5R,6R)-6-{3-[(E)-2-(4-chloro-phenyl)-vinyl]-ureido}-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylate 
• 132606-72-5 4-chlorocinnamyl isocyanate 

Relevant articles and documents

Chiral phosphoric acid catalyzed enantioselective annulation of acyclic enecarbamates to: In situ -generated ortho -quinone methides

The first organocatalytic asymmetric reaction of acyclic enecarbamates with o-quinone methides is disclosed. BINOL-based phosphoric acid catalysts were found to be suitable for the annulation reaction. With 10 mol% of the TRIP catalyst, high yields as well as excellent diastereo- and enantioselectivities are achieved for a variety of 2,3,4-trisubstituted chroman products.

Synthesis and Evaluation of Ureido- and Vinylureidopenicillins as Inhibitors of Intraruminal Lactic Acid Production

A series of 14 vinylureidopenicillins and a series of 9 ureidopenicillins were prepared by reaction of 6-aminopenicillanic acid with vinyl isocyanates and isocyanates.These compounds were evaluated for their potential to protect ruminants against lactic a