115224-13-0

Basic information

• Product Name: (R)-A-PHENYL-3-BUTENAMINE
• Synonyms: (R)-A-PHENYL-3-BUTENAMINE;(1R)-1-PHENYLBUT-3-EN-1-AMINE;(1R)-1-PHENYLBUT-3-EN-1-AMINE-HCL
• CAS NO: 115224-13-0
• Molecular Formula: C₁₀H₁₃N
• Molecular Weight: 147.22
• Mol File: 115224-13-0.mol
• Article Data: 42

Chemical Properties

• Boiling Point: 219.7°C at 760 mmHg
• Flash Point: 90.9°C
• Appearance: /
• Density: 0.951g/cm³
• Vapor Pressure: 0.118mmHg at 25°C
• Refractive Index: 1.536
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• CAS DataBase Reference: (R)-A-PHENYL-3-BUTENAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-A-PHENYL-3-BUTENAMINE(115224-13-0)
• EPA Substance Registry System: (R)-A-PHENYL-3-BUTENAMINE(115224-13-0)

Safety Data

• Hazardous Substances Data: 115224-13-0(Hazardous Substances Data)

Usage

General Description

(R)-A-PHENYL-3-BUTENAMINE, also known as (R)-1-amino-1-phenyl-3-buten-2-ol, is a chemical compound with the formula C10H13N. It is an organic compound that belongs to the class of amines and is primarily used as an intermediate for the synthesis of pharmaceuticals and agrochemicals. It is a chiral compound, meaning it has a non-superimposable mirror image, and it exists in two enantiomeric forms, (R)- and (S)-. (R)-A-PHENYL-3-BUTENAMINE is commonly utilized in the production of various drugs, including potential antitumor and antidepressant medications. Additionally, it is used in the synthesis of chiral ligands and catalysts for asymmetric transformations in organic chemistry. (R)-A-PHENYL-3-BUTENAMINE is an important building block with versatile applications in the pharmaceutical and chemical industries.

InChI:InChI=1/C10H13N/c1-2-6-10(11)9-7-4-3-5-8-9/h2-5,7-8,10H,1,6,11H2/t10-/m1/s1

Upstream product

• 53075-84-6 benzaldehyde (E)-N-benzenesulfenylimine 
• 85116-38-7 (+)-diisopinocampheylallylborane 
• 10229-53-5 (E)-benzaldehyde O-methyloxime 
• 124821-92-7 d-B-allylbis(2-isocaranyl)borane 
• 108-21-4 Isopropyl acetate 
• 4383-23-7 1-phenyl-but-3-enylamine 
• 3938-96-3 ethyl 2-methoxyacetate 
• 17599-61-0 N-benzylidene-1,1,1-trimethylsilanamine 
• 14850-88-5 benzoylhydrazone of benzaldehyde 
• 130887-64-8 (S)-1-phenylbut-3-en-1-amine hydrochloride 
• 120419-97-8 (E)-N-benzylidene-1,1,1-trimethylsilanamine 
• 107-05-1 3-chloroprop-1-ene 
• 2622-05-1 allylmagnesium bromide 
• 851727-29-2 (R)-N-(1-phenyl-3-butenyl)benzenesulfonamide 

Downstream Products

• 333380-82-8 N-((S)-1-phenylbut-3-enyl)acetamide 
• 949021-19-6 (S)-N-(1-phenyl-3-buten-1-yl)propenamide 
• 135865-77-9 (S)-N-(tert-Butoxycarbonyl)-1-phenyl-3-butenylamine 
• 1220121-32-3 C₁₄H₁₉NO 
• 231617-04-2 (R)-N-acetyl-4-amino-4-phenyl-1-butene 
• 1357361-01-3 6-(bromomethyl)-4-phenyl-1,3-oxazinan-2-one 
• 326477-54-7 6-phenyl-5,6-dihydro-2,4(1H,3H)-pyridinedione 
• 1449466-90-3 (S)-N-(t-butoxycarbonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-phenyl-butan-1-amine 

Relevant articles and documents

Synthesis and catalytic application of chiral 1,1′-bi-2-naphthol-and biphenanthrol-based pincer complexes: Selective allylation of sulfonimines with allyl stannane and allyl trifluoroborate

(Chemical Equation Presented) New easily accessible 1,1′-bi-2- naphthol- (BINOL-) and biphenanthrol-based chiral pincer complex catalysts were prepared for selective (up to 85% enantiomeric excess) allylation of sulfonimines. The chiral pincer complexes w

Enantioselective Strecker and Allylation Reactions with Aldimines Catalyzed by Chiral Oxazaborolidinium Ions

Chiral oxazaborolidinium ion (COBI)-catalyzed enantioselective nucleophilic addition reactions of aldimines using tributyltin cyanide and allyltributylstannane have been developed. Various α-aminonitriles and homoallylic amines were synthesized in high yi

Copper-catalyzed asymmetric allylation of chiral N-tert-butanesulfinyl imines: Dual stereocontrol with nearly perfect diastereoselectivity

Copper-catalyzed asymmetric allylation of chiral N-tert-butanesulfinyl imines has been described. Dual stereocontrol, through the combination of a chiral auxiliary and a chiral copper complex, has played an important role in achieving the nearly perfect d