14717-30-7

Basic information

• Product Name: Benzene, 1-chloro-2-(1-pentenyl)-
• CAS NO: 14717-30-7
• Molecular Formula: C11H13Cl
• Molecular Weight: 180.677
• Mol File: 14717-30-7.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Benzene, 1-chloro-2-(1-pentenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-chloro-2-(1-pentenyl)-(14717-30-7)
• EPA Substance Registry System: Benzene, 1-chloro-2-(1-pentenyl)-(14717-30-7)

Safety Data

• Hazardous Substances Data: 14717-30-7(Hazardous Substances Data)

Upstream product

• 925-90-6 ethylmagnesium bromide 
• 881404-67-7 (E)-1-(3-bromoprop-1-en-1-yl)-2-chlorobenzene 
• 557-20-0 diethylzinc 
• 7295-44-5 4'-bromovalerophenone 
• 89-98-5 2-chloro-benzaldehyde 
• 1009-14-9 phenyl butyl ketone 
• 502-56-7 nonanone-5 
• 693-03-8 n-butyl magnesium bromide 

Downstream Products

• 1342886-89-8 2-(2-chlorophenyl)pentanal 
• 1342886-78-5 C₁₁H₁₄BrClO 
• 14401-81-1 1,12-Bis-<2-chlor-phenyl>-dodecen-(6) 
• 14491-42-0 1,12-Bis-(2-chlorphenyl)-dodecin-⁽⁶⁾ 
• 14491-45-3 1-Brom-5-(2-chlor-phenyl)-pentan 
• 14469-87-5 5-(2-chlorophenyl)pentan-1-ol 

Relevant articles and documents

P-Chiral Monophosphorus Ligands for Asymmetric Copper-Catalyzed Allylic Alkylation

Asymmetric copper-catalyzed allylic alkylation between allyl bromides and alkyl Grignard reagents using a P-chiral monophosphorus ligand is described. A range of terminal olefins bearing tertiary or quaternary carbon centers were formed in good branched/linear selectivities and excellent enantioselectivities at copper loadings as low as 0.5 mol %.

Highly regioselective asymmetric copper-catalyzed allylic alkylation with dialkylzincs using monodentate chiral spiro phosphoramidite and phosphite ligands

The copper complexes of chiral spiro phosphoramidite and phosphite ligands were found to be effective catalysts in the asymmetric allylic alkylations of cinnamyl halides with dialkylzincs. The allylic alkylation products were obtained in high regioselecti

Synthesis of (E)-1-Aryl-1-alkenes via a Novel BF3·OEt2-Catalyzed Aldol-Grob Reaction Sequence

The reactions of aromatic aldehydes with ketones in the presence of various acids were examined. The reactions generate (E)-1-aryl-1-alkenes in the presence of boron trifluoride diethyl etherate in nonnucleophilic solvents.