70576-29-3

Basic information

• Product Name: Benzaldehyde, 2-(3-butenyl)-
• CAS NO: 70576-29-3
• Molecular Formula: C11H12O
• Molecular Weight: 160.216
• Mol File: 70576-29-3.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 2-(3-butenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 2-(3-butenyl)-(70576-29-3)
• EPA Substance Registry System: Benzaldehyde, 2-(3-butenyl)-(70576-29-3)

Safety Data

• Hazardous Substances Data: 70576-29-3(Hazardous Substances Data)

Upstream product

• 89-95-2 2-methyl-benzyl alcohol 
• 106-95-6 allyl bromide 
• 529-20-4 2-methylphenyl aldehyde 
• 71813-50-8 1-bromo-2-(but-3-enyl)benzene 
• 68-12-2 N,N-dimethyl-formamide 
• 142-25-6 N,N',N'-trimethylenediamine 
• 5162-44-7 1-bromo-4-butene 
• 35849-09-3 o-bromobenzaldehyde dimethyl acetal 
• 121089-46-1 (2-(but-3-en-1-yl)phenyl)methanol 
• 89730-30-3 2-(but-3-en-1-yl)benzoic acid 
• 118-90-1 ortho-methylbenzoic acid 
• 70576-27-1 (1-Hydroxy-1,2,3,4-tetrahydro-naphthalen-2-ylmethyl)-trimethyl-ammonium; iodide 

Downstream Products

• 121089-48-3 (E)-N-(2-(but-3-en-1-yl)benzylidene)prop-2-en-1-amine 
• 184697-61-8 1-(but-3-enyl)-2-(2,2-dibromovinyl)benzene 
• 1119036-84-8 1-(2-but-3-enylphenyl)-3-(trimethylsilyl)prop-2-yn-1-ol 
• 1207288-97-8 methyl 3-(2-(but-3-enyl)phenyl)propiolate 
• 1207288-98-9 3-(2-(but-3-enyl)phenyl)propiolic acid 
• 1314234-83-7 [2-(but-3-en-1-yl)phenyl](3,3-dimethylcycloprop-1-en-1-yl)methanol 

Relevant articles and documents

Nickel-Catalyzed Intramolecular Hydroalkenylation of Imines

A ligand-enabled nickel-catalyzed intramolecular hydroalkenylation of imines with unactivated alkenes has been developed. A variety of five- and six-membered cyclic allylic amines were synthesized in high yields. The use of both wide-bite-angle diphosphine ligand and Br?nsted acid is crucial for realizing the reaction. Preliminary investigation of the asymmetric intramolecular hydroalkenylation of imines shows promising potential for the application of the method in the synthesis of enantio-enriched cyclic allylic amines.

Application of Dehydroabietic Acid in Palladium-Catalysed Enyne Cycloisomerisation

Dehydroabietic acid (DAA) promotes palladium(0)-catalysed cyclisations of arene-tethered 1,7-enynols and 1,m-enynoates (m=6,7) to give fused carbocyclic dienes. 6,6,6,5-Tetracyclic lactones are accessible by one-pot cycloisomerisation/Diels–Alder reaction

Pyrazolopyrimidine Macrocycles as Inhibitors of Human Immunodeficiency Virus Replication

The disclosure generally relates to compounds of formula I, including compositions and methods for treating human immunodeficiency virus (HIV) infection. The disclosure provides novel inhibitors of HIV, pharmaceutical compositions containing such compound