512789-12-7

Basic information

• Product Name: Carbonic acid, (2E)-3-(2-methoxyphenyl)-2-propenyl methyl ester
• CAS NO: 512789-12-7
• Molecular Formula: C12H14O4
• Molecular Weight: 222.241
• Mol File: 512789-12-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Carbonic acid, (2E)-3-(2-methoxyphenyl)-2-propenyl methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbonic acid, (2E)-3-(2-methoxyphenyl)-2-propenyl methyl ester(512789-12-7)
• EPA Substance Registry System: Carbonic acid, (2E)-3-(2-methoxyphenyl)-2-propenyl methyl ester(512789-12-7)

Safety Data

• Hazardous Substances Data: 512789-12-7(Hazardous Substances Data)

Upstream product

• 60125-24-8 (E)-3-(2-methoxyphenyl)propenal 
• 1504-61-6 (E)-3-(2-methoxyphenyl)prop-2-en-1-ol 
• 79-22-1 methyl chloroformate 

Downstream Products

• 1087162-42-2 tert-butyl 2-cyano-3-(2-methoxyphenyl)pent-4-enoate 
• 1087162-25-1 (2S,3R)-ethyl 2-(diphenylmethyleneamino)-3-(2-methoxyphenyl)pent-4-enoate 
• 1087162-30-8 (2R,3R)-ethyl 2-(diphenylmethyleneamino)-3-(2-methoxyphenyl)pent-4-enoate 
• 1087162-20-6 N,N-diethyl-1-(2-methoxyphenyl)prop-2-en-1-amine 
• 1239597-36-4 (E)-ethyl 5-(2-methoxyphenyl)-2-methylenepent-4-enoate 
• 1164283-85-5 C₁₅H₁₃ClN₄O 
• 1164283-72-0 (R)-6-chloro-9-(1-(2-methoxyphenyl)allyl)-9H-purine 
• 1164282-90-9 (R)-1-(1-(2-methoxyphenyl)allyl)-1H-benzo[d]imidazole 
• 1161928-87-5 C₁₈H₁₉NO 

Relevant articles and documents

Application of iridium catalyzed allylic substitution reactions in the synthesis of branched tryptamines and homologues via tandem hydroformylation- Fischer indole synthesis

Combination of enantioselective allylation reactions with a tandem hydroformylation-Fischer indole synthesis sequence as a highly diversity-oriented strategy for the synthesis of tryptamines and homologues was explored. This modular approach allows the su

Enantioselective allylation of aromatic amines after in situ generation of an activated cyclometalated iridium catalyst

Highly regio- and enantioselective allylation of aromatic amines is observed when a cyclometalated Ir-phosphoramidite complex is generated in situ (see scheme). The active catalyst can be formed from [{Ir(cod)Cl}2] and ligand L with a volatile alkylamine prior to addition of the reagents or upon use of a tertiary amine additive.