4226-59-9

Basic information

• Product Name: 2-Propen-1-amine, 3-phenyl-, (Z)-
• Synonyms: 3-phenylallylamine;3-phenyl-2Z-propen-1-amine;cis-Cinnamylamine;Cinnamylamine
• CAS NO: 4226-59-9
• Molecular Formula: C9H11N
• Molecular Weight: 133.193
• Mol File: 4226-59-9.mol
• Article Data: 49

Chemical Properties

• Boiling Point: 84 - 87 °C (1.8 mmHg)
• Density: 0.993±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2-Propen-1-amine, 3-phenyl-, (Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propen-1-amine, 3-phenyl-, (Z)-(4226-59-9)
• EPA Substance Registry System: 2-Propen-1-amine, 3-phenyl-, (Z)-(4226-59-9)

Safety Data

• Hazardous Substances Data: 4226-59-9(Hazardous Substances Data)

Upstream product

• 13372-81-1 (1E,2E)-cinnamaldehyde oxime 
• 21087-29-6 trans-3-phenylprop-2-enyl chloride 
• 33143-51-0 (E)-N-(3-phenylallyl)carbamic acid methyl ester 
• 4335-61-9 2-[(Z)-3-phenylprop-2-enyl]-2,3-dihydro-1H-isoindole-1,3-dione 
• 1504-58-1 3-Phenyl-2-propyn-1-ol 
• 591-50-4 iodobenzene 
• 56866-32-1 2-[(E/Z)-3-phenylprop-2-enyl]-2,3-dihydro-1H-isoindole-1,3-dione 
• 100-52-7 benzaldehyde 
• 89996-00-9 (2-aminoethyl)triphenylphosphonium bromide salt 
• 4192-77-2 ethyl cinnamate 
• 4187-87-5 1-Phenyl-2-propyn-1-ol 
• 300-57-2 allylbenzene 
• 59336-59-3 cinnamaldehyde oxime 
• 52966-67-3 N-cinnamyl-trifluoroacetamide 

Downstream Products

• 75606-32-5 2-((E)-3-Phenyl-allylamino)-ethanethiol 
• 138354-53-7 1H-Indole-2-carboxylic acid ((E)-3-phenyl-allyl)-amide 
• 126070-18-6 2-(3-phenyl-2-propenyl)-1,3(2H,4H)-isoquinolinedione 
• 120990-23-0 N-(phenylmethylidene)-N-[(E)-3-phenylprop-2-enyl]amine 
• 492435-14-0 (S)-2-Hydroxy-2-phenyl-N-((E)-3-phenyl-allyl)-acetamide 
• 908351-76-8 ((S)-5-Benzyloxycarbonylamino-6-hydroxy-6-{5-[4-((E)-3-phenyl-allylcarbamoyl)-benzyl]-[1,2,4]oxadiazol-3-yl}-hexyl)-carbamic acid tert-butyl ester 
• 129906-97-4 4-(tert-butyl)-N-cinnamylbenzamide 

Relevant articles and documents

PROTEIN LABELLING

A process for labelling a target protein, such as a target enzyme, such as a deubiquitinating enzyme (DUB). The process comprises providing a probe-protein complex comprising a probe and the target protein. The probe comprises a recognition element and a

Copper-Catalyzed Aerobic Oxidation of Amines to Benzothiazoles via Cross Coupling of Amines and Arene Thiolation Sequence

A one-pot three-component synthesis of benzothiazoles has been developed using the copper-catalyzed aerobic cross coupling of amines followed by arene thiolation using elemental sulfur. The dual roles of elemental sulfur and CuCl(OH)-TMEDA in the aerobic amine oxidation and the aniline thiolation enable the facile access to benzothiazole derivatives from readily available starting materials. The operational simplicity of the current promiscuous catalyst system suggests the high synthetic potential in the preparation of heterocyclic compounds. (Figure presented.).