970-86-5

Upstream product

• 1233-73-4 Benzophenone-4,4'-dicarboxylic acid dimethyl ester 
• 619-44-3 methyl 4-iodobenzoate 
• 1571-08-0 methyl 4-formylbenzoate 
• 368421-80-1 (4-(methoxycarbonyl)phenyl)magnesium chloride 
• 1092-70-2 methyl 4-[(4-methoxycarbonylphenyl)methyl]benzoate 
• 101-81-5 Diphenylmethane 
• 619-58-9 4-iodobenzoic acid 
• 124-38-9 carbon dioxide 
• 50793-48-1 bis(p-methoxycarbonylphenyl)bromomethane 

Downstream Products

• 120467-74-5 bis(p-methoxycarbonylphenyl)methyl isovalerate 
• 1233-73-4 Benzophenone-4,4'-dicarboxylic acid dimethyl ester 
• 875210-90-5 O-[-6-(3,5-didecyloxyphenyloxy)hexyl]-4,4'-bis(methoxycarbonylphenyl)methanone oxime 
• 912806-45-2 O-[6-(3-decyloxyphenyloxy)hexyl]-4,4'-bis(methoxycarbonylphenyl)methanone oxime 
• 875210-87-0 4,4'-bis(methoxycarbonylphenyl)methanone oxime 
• 120467-75-6 bis(p-methoxycarbonylphenyl)methyl trichloroacetate 

Relevant academic research and scientific papers

Non-Glycosidic and Non-Peptidic Select Inhibitors, and the Use Thereof

A new class of non-glycosidic and non-peptidic inhibitors of selectins with low molecular weight according to the general formula 1 is described, as well as methods for their production. These compounds represent a new class of non-toxic, in vivo anti-inf

A novel class of potent nonglycosidic and nonpeptidic pan-selectin inhibitors

An early step of the inflammatory response, the rolling of leukocytes on activated endothelial cells, is mediated by selectin/carbohydrate interactions. The tetrasaccharide sialy LewisX is a ligand for E-, P-, and L-selectin and therefore serve

NON-GLYCOSIDIC AND NON-PEPTIDIC SELECT INHIBITORS, AND THE USE THEREOF

The invention relates to a category of non-glycosidic and non-peptidic select inhibitors of general formula (1), with a low molecular weight, and to a method for the production thereof. Said category is a category of non-toxic select inhibitors having an

Observation of intramolecular dimer radical anion of 1,1-diarylmethanols bearing electron withdrawing groups at room temperature

Transient absorption measurement of radical anions of 1,1-diarylmethanols bearing electron-withdrawing groups in dimethyl-formamide at room temperature has revealed that symmetric compounds form intramolecular dimer radical anions as an intermediate of th

SYNTHESIS OF JUVABIONE ANALOGUES

Alkylation of various β-ketoesters IIIa-d with bis(p-methoxycarbonylphenyl)bromomethane (II) and bis(p-chlorophenyl)bromomethane (VI) followed by cleavage of ethoxycarbonyl group or hydrolysis and esterification gave methoxycarbonylphenyl and chlorophenyl analogues of ar-juvabione, respectively.Condensation of bis(p-methoxycarbonylphenyl)methanol (IX) with isovaleryl and trichloroacetyl chloride gave isovalerate X and trichloroacetate XI, respectively, while the condensation of bis(p-chlorophenyl)methanol (XII) with isovaleryl chloride and citronellyl bromide yieldedisovalerate XIII and citronellyl ether XIV, respectively.The methoxycarbonylation of aryl-alkyl ketones XVa-d with oxalyl chloride and treatment with methanol furnished various ar-juvabione analogues XVIa-d.The compounds Vb, Vc, Vd, XVIb, and XVIc showed high activity against Dysdercus koenigii at 1μg concentration.