1393683-26-5

Basic information

• Product Name: 1-(3-ethylpent-2-en-1-yl)-4-methoxybenzene
• Synonyms: 1-(3-ethylpent-2-en-1-yl)-4-methoxybenzene
• CAS NO: 1393683-26-5
• Molecular Weight: 204.312
• Mol File: 1393683-26-5.mol

Chemical Properties

• CAS DataBase Reference: 1-(3-ethylpent-2-en-1-yl)-4-methoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-ethylpent-2-en-1-yl)-4-methoxybenzene(1393683-26-5)
• EPA Substance Registry System: 1-(3-ethylpent-2-en-1-yl)-4-methoxybenzene(1393683-26-5)

Safety Data

• Hazardous Substances Data: 1393683-26-5(Hazardous Substances Data)

Upstream product

• 104-92-7 1-bromo-4-methoxy-benzene 
• 21378-06-3 1-bromo-3-ethylpent-2-ene 
• 15249-93-1 ethyl 3-ethylpent-2-enoate 
• 96-22-0 pentan-3-one 
• 28495-72-9 4-methyl-N’-(pentan-3-ylidene)-benzenesulfonohydrazide 
• 72316-18-8 (E)-2-(4-methoxyphenyl)vinylboronic acid 

Relevant articles and documents

Nickel-Catalyzed Regioselective Reductive Cross-Coupling of Aryl Halides with Polysubstituted Allyl Halides in the Presence of Imidazolium Salts

The nickel-catalyzed direct reductive cross-coupling of aryl halides with readily accessible polysubstituted allyl halides provides an efficient method for preparing diverse allylated arenes under mild conditions. Both allyl bromides and allyl chlorides are compatible with the transformation.

Olefination of carbonyl compounds through reductive coupling of alkenylboronic acids and tosylhydrazones

The partners decide: The C-C bond-forming reductive cross-coupling of alkenylboronic acids and tosylhydrazones takes place under mild reaction conditions without the need of a metal catalyst, thus giving rise to olefination-type products (see scheme). The position of the double bond in the product is determined by the structure of the coupling partners. Copyright