107224-27-1

Basic information

• Product Name: (E)-undec-1-en-1-ylbenzenecolorless
• Synonyms: (E)-undec-1-en-1-ylbenzenecolorless
• CAS NO: 107224-27-1
• Molecular Weight: 230.393
• Mol File: 107224-27-1.mol
• Article Data: 20

Chemical Properties

• CAS DataBase Reference: (E)-undec-1-en-1-ylbenzenecolorless(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-undec-1-en-1-ylbenzenecolorless(107224-27-1)
• EPA Substance Registry System: (E)-undec-1-en-1-ylbenzenecolorless(107224-27-1)

Safety Data

• Hazardous Substances Data: 107224-27-1(Hazardous Substances Data)

Upstream product

• 6990-68-7 1-phenylundecan-1-ol 
• 3043-65-0 (phenyl)methyl 1-phenyl-1H-tetrazol-5-yl sulfone 
• 112-31-2 caprinaldehyde 
• 591-50-4 iodobenzene 
• 75456-63-2 undec-1-enal dimethyl acetal 
• 1424273-59-5 O-phenyl O-(1-phenylundecyl) carbonothioate 
• 53210-25-6 undec-10-en-1-ylbenzene 
• 5123-13-7 5,5-dimethyl-2-phenyl-1,3,2-dioxaborinane 
• 75039-84-8 (E)-undec-2-en-1-ol 
• 1327239-03-1 (E)-1-methoxyundec-2-ene 
• 4407-36-7 (2E)-3-phenyl-2-propen-1-ol 
• 24808-73-9 (E)-(3-methoxyprop-1-en-1-yl)benzene 
• 17049-49-9 octylmagnesium bromide 
• 100-58-3 phenylmagnesium bromide 

Downstream Products

• 61439-50-7 11-phenylundecylalcohol 
• 101025-08-5 1-bromo-11-phenylundecane 
• 14401-84-4 1,14-Diphenyl-tetradecadien-(1,3) 

Relevant articles and documents

METHODS OF BORYLATION AND USES THEREOF

The present invention relates, in general terms, to methods of borylation and uses thereof. In particular, the present invention provides a method of borylating an alkene compound by contacting the compound with a boron compound, a Fe pre-catalyst and a protic additive. The borylation occurs at a vicinal (β) position to an electron donating or electron withdrawing moiety of the compound.

Development of unique dianionic Ir(III) CCC pincer complexes with a favourable spirocyclic NHC framework

A new type of dianionic Ir(III) CCC pincer complexes (SNHC-Ir, 1a-1c) is successfully designed and synthesized by developing a one-step methodology, which involves an initial coordination of Ir(I) with the NHC and subsequent metallation of double sp2C- H bonds. This method is considerably useful over those reported by using strong coordination ligand or carbonic anion exchange, and would provide an alternative efficient template of organometallics synthesis. Experimental and density functional theory (DFT) calculation results indicate that the spirocyclic framework is a favourable factor for the facile formation and stabilization of these complexes. Primary investigation shows that chloride 1b can well catalyze homo and hetero addition of styrene derivatives and remote olefin isomerization, which represents the first catalytic application of the dianionic CCC pincer complexes.

Highly E-Selective, Stereoconvergent Nickel-Catalyzed Suzuki-Miyaura Cross-Coupling of Alkenyl Ethers

An improved method for the nickel-catalyzed Suzuki-Miyaura cross-coupling of alkenyl ethers is reported. This stereoconvergent protocol allows for the utilization of a wide range of alkenyl ethers and aryl boronic esters for the synthesis of variously sub