79249-70-0

Upstream product

• 67-56-1 methanol 
• 54118-63-7 2-Amino-4-tert-butyl-phenol; hydrochloride 
• 1199-46-8 2-amino-4-tert-butylphenol 
• 74-88-4 methyl iodide 

Downstream Products

• 80816-96-2 N-cinnamyl-2-hydroxy-NN-dimethyl-5-t-butylanilinium bromide 
• 79249-76-6 2-hydroxy-NN-dimethyl-N-(2-methylallyl)-5-t-butylanilinium bromide 
• 79249-75-5 N-allyl-2-hydroxy-NN-dimethyl-5-t-butylanilinium bromide 
• 80817-12-5 2-cinnamyloxy-NN-dimethyl-5-t-butylaniline 
• 79249-83-5 NN-dimethyl-N-(2-methylallyl)-5-t-butylanilinium-2-olate 
• 79249-82-4 N-allyl-NN-dimethyl-5-t-butylanilinium-2-olate 
• 80817-23-8 N-<1,1-(2)H2>allyl-2-hydroxy-NN-dimethyl-5-t-butylanilinium toluene-p-sulphonate 

Relevant academic research and scientific papers

SYNTHESIS OF SUBSTITUTED AMIDOBENZOATE COMPOUNDS, THE COMPOUNDS OBTAINED AND THE USE THEREOF AS PHTHALATE FREE INTERNAL ELECTRON DONOR FOR POLYMERIZATION OF OLEFINS

The present invention relates to a compound according to Formula (I) wherein R1 is a hydrocarbyl group selected from the group consisting of alkyl, alkenyl, aryl, aralkyl, and alkylaryl groups, and one or more combinations thereof; wherein Rsu

AMIDE COMPOUNDS

A compound of the formula (I) wherein R1 is hydrogen, lower alkyl, lower alkenyl, halo(lower)alkyl, cyclo(lower)alkyl, lower alkoxy, lower alkylthio, acyl, optionally substituted aryl or NR3R4; R2 is hydrogen; or aryl or heteroaryl, each of which may be substituted; X is direct bond or bivalent residue derived from piperazine; Y is -(A1)n#191-(A2?)?m#191-, wherein n and m are independently 0 or 1); is bivalent residue derived from arene or heteroarene; and is bivalent residue derived from arene or heteroarene, or a salt thereof. The compound of the present invention and a salt thereof inhibit apolipoprotein B (Apo B) secretion and are useful as a medicament for prophylactic and treatment of diseases or conditions resulting from elevated circulating levels of Apo B.

Base Catalysed Rearrangements involving Ylide Intermediates. Part 13. Further Rearrangements of 2-Oxidoanilinium Ylides

The 2-oxidoanilinium ylides (7) rearrange on heating to give the ethers (10) together with the dienones (8) and the phenols (11) for cases where the aromatic ring has a 5-alkyl substituent or a mixture of the dienones (8) and (12) for cases where the aromatic ring is 3,5-disubstituted.A study of the deuteriated ylides (25) shows that these reactions involve competing concerted and radical-pair processes.The base-catalysed rearrangements of the 2-hydroxy-N-pentadienylanilinium salts (33) give the ethers (34) and the phenols (35): these products result from competing concerted and rearrangements of the ylides (36) corresponding to the salts (33).