1188296-81-2

Basic information

• Product Name: 1-(1,2-dichloroethenyloxy)-4-methoxybenzene
• Synonyms: 1-(1,2-dichloroethenyloxy)-4-methoxybenzene
• CAS NO: 1188296-81-2
• Molecular Weight: 219.067
• Mol File: 1188296-81-2.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 1-(1,2-dichloroethenyloxy)-4-methoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(1,2-dichloroethenyloxy)-4-methoxybenzene(1188296-81-2)
• EPA Substance Registry System: 1-(1,2-dichloroethenyloxy)-4-methoxybenzene(1188296-81-2)

Safety Data

• Hazardous Substances Data: 1188296-81-2(Hazardous Substances Data)

Upstream product

• 79-01-6 Trichloroethylene 
• 150-76-5 4-methoxy-phenol 

Downstream Products

• 75290-86-7 methoxy-4-(prop-2-ynyloxy)benzene 
• 1188296-85-6 3-(4-methoxyphenoxy)prop-2-yn-1-ol 
• 1188296-86-7 4-(4-methoxyphenoxy)but-3-yn-2-ol 
• 1188296-87-8 1-(4-methoxyphenoxy)-pent-1-yn-3-ol 
• 1188296-88-9 1-(4-methoxyphenoxy)-4,4-dimethylpent-1-yn-3-ol 
• 1421257-50-2 (R)-1-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-3-(4-methoxyphenoxy)propan-1-ol 
• 1421257-52-4 (S,Z)-1-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-3-(4-methoxyphenoxy)allyl 2-(((2R,4S,5R)-2-(4-chlorophenyl)-4-vinyl-1,3-dioxan-5-yl)oxy)acetate 
• 1421257-58-0 methyl (2R,3R,E)-2-(((2R,4S,5R)-2-(4-chlorophenyl)-4-vinyl-1,3-dioxan-5-yl)oxy)-3-(4-methoxyphenoxy)hex-5-enoate 
• 1421257-49-9 (S,Z)-1-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-3-(4-methoxyphenoxy)prop-2-en-1-ol 
• 1421257-48-8 (R,Z)-1-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-3-(4-methoxyphenoxy)prop-2-en-1-ol 

Relevant articles and documents

Asymmetric addition of aryloxy ethynyl lithium derivatives to N-sulfinyl imines

Aryloxy ethynyl lithium species can be generated in diethyl ether and efficiently added to aliphatic and aromatic N-sulfinyl imines in THF, affording aryloxypropargyl sulfinamides in good yield, and in most cases high diastereoselectivity. The diastereose

Alkynoxy-directed C-H functionalizations: Palladium(0)-catalyzed annulations of alkynyl aryl ethers with alkynes

Palladium(0)-catalyzed insertion/annulation sequence between aryl silylethynyl ethers and internal alkynes was found to proceed through activation of ortho-C-H bonds assisted by alkynoxy groups and gave stereoselectively (Z)-2-silylmethylenechromenes. The

An Ireland-Claisen rearrangement/RCM based approach for the construction of the EF-ring of ciguatoxin 3C

The EF-ring of ciguatoxin 3C, a marine toxin from the dinoflagellate Gambierdiscus toxicus, was stereoselectively synthesized by iterative use of a cyclic ether formation process based on chirality-transferring Ireland-Claisen rearrangement and ring-closing olefin metathesis.