94413-73-7

Basic information

• Product Name: 2-Propenoic acid, 2-azido-3-phenyl-, methyl ester
• CAS NO: 94413-73-7
• Molecular Formula: C10H9N3O2
• Molecular Weight: 203.2
• Mol File: 94413-73-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-Propenoic acid, 2-azido-3-phenyl-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenoic acid, 2-azido-3-phenyl-, methyl ester(94413-73-7)
• EPA Substance Registry System: 2-Propenoic acid, 2-azido-3-phenyl-, methyl ester(94413-73-7)

Safety Data

• Hazardous Substances Data: 94413-73-7(Hazardous Substances Data)

Upstream product

• 4504-27-2 1-azidopropan-2-one 
• 100-52-7 benzaldehyde 
• 103-26-4 methyl cinnamate 
• 1816-92-8 Methyl azidoacetate 

Downstream Products

• 1202-04-6 indole-2-carboxylic acid methyl ester 
• 1380411-90-4 methyl 1-(4-chlorophenyl)-2,4-diphenyl-1H-imidazole-5-carboxylate 
• 1262779-18-9 N-((1-allylindol-2-yl)methyl)-4-methylbenzenesulfonamide 
• 1529807-01-9 9-allyl-4'-methyl-1',2-ditosyl-1,1',2,3,5',9-hexahydro-spiro[pyrido[3,4-b]indole-4,2'-pyrrole] 
• 1529806-81-2 N-((1-allyl-1H-indol-2-yl)methyl)-4-methyl-N-(3-(2-methyl-1-tosylaziridin-2-yl)prop-2-ynyl)benzenesulfonamide 
• 1621106-07-7 methyl 4-phenyl-3-(p-tolyl)isoxazole-5-carboxylate 
• 27000-00-6 methyl 2-hydroxy-3-phenylpropionate 
• 13673-95-5 (S)-methyl 2-hydroxy-3-phenylpropanoate 
• 13674-16-3 methyl 2-hydroxy-3-phenylpropanoate 
• 1372411-96-5 methyl 1,5-dioxo-4-phenyl-2,5-dihydro-1H-benzo[c]azepine-3-carboxylate 
• 1372411-80-7 methyl 5-hydroxy-1-oxo-4-phenyl-2,5-dihydro-1H-benzo[c]azepine-3-carboxylate 
• 1345509-75-2 methyl 1,2,4-triphenyl-1H-imidazole-5-carboxylate 
• 128070-30-4 (E)-3-Phenyl-2-(3-phenyl-ureido)-acrylic acid methyl ester 

Relevant articles and documents

A telescoped protocol for the synthesis of new pyrrolo [3,4-d]pyridazinones by cascade reactions

A new one-pot method, for the synthesis of polysubstituted pyrrolo[3,4-d]pyridazinones, is presented. The protocol consists in cascade reactions performed in the same media: (i) the thermal in situ pyrrole formation by the reaction of vinyl azides with 1,

Gold(I)-catalyzed rearrangement of alkynylaziridine indoles for the synthesis of spiro-tetrahydro-β-carbolines

Functionalized spiro-tetrahydro-β-carbolines were formed by an efficient gold(I)-catalyzed rearrangement reaction of alkynylaziridine indoles. The reaction involved a Friedel-Crafts type intramolecular reaction of alkynylaziridine indoles, following by hydroamination of aminoallene intermediate.

AMINO ACIDS AS SYNTHONS FOR HETEROCYCLES. FORMATION OF 1,2,4-TRIAZINE DERIVATIVES

Transformation of the amino group of amino acids into an amidine and subsequent treatment with hydrazine leads to 1,2,4-triazine-6(1H)-ones.The method described is a new synthetic approach.Unsaturated amino acids gave imidazol-5-one derivatives after the