71819-90-4

Upstream product

• 16700-55-3 2,6-dimethoxybenzyl alcohol 
• 2065-27-2 methyl 2,6-dimethoxybenzoate 

Downstream Products

• 107890-06-2 2-(2,6-Dimethoxy-benzyl)-6-methoxy-2,3,4,9-tetrahydro-1H-β-carboline 
• 91622-93-4 5-<(2,6-dimethoxyphenyl)methyl>-6a,7,8,9-tetrahydropyrido<3,2-e>pyrrolo<1,2-a>pyrazin-6(5H)-one 
• 15561-50-9 2-(2,6-dimethoxyphenyl)acetic acid 
• 477573-11-8 5-(2,6-Dimethoxy-phenylmethanesulfonyl)-1,3-dihydro-indol-2-one 
• 15256-41-4 O,N-Bis-(2,6-dimethoxy-benzyl)-hydroxylamin 
• 91622-96-7 5-<(2,6-dimethoxyphenyl)methyl>-6a,7,8,9-tetrahydropyrido<3,2-e>pyrrolo<1,2-a>pyrazine 
• 15258-37-4 N-(2,6-Dimethoxy-benzyl)-N-(2,6-dimethoxy-benzoyl)-carbamidsaeure-ethylester 
• 91623-04-0 5-<(2,6-dimethoxyphenyl)methyl>-1,2,3,3a-tetrahydropyrrolo<1,2-a>quinoxalin-4(5H)-one 

Relevant academic research and scientific papers

PYRAZOLO[4,3-d]PYRIMIDINE DERIVATIVES AND METHODS OF USE THEREOF FOR THE TREATMENT OF CELLULAR PROLIFERATIVE DISORDERS

The present invention relates to novel Pyrazolo[4,3-d]Pyrimidine Derivatives of Formula (I): (I) and pharmaceutically acceptable salts thereof, wherein R1, R2 and R3 are as defined herein. The present invention also relate

Phosphorylation Organocatalysts Highly Active by Design

The activity of nucleophilic organocatalysts for alcohol/phenol phosphorylation was enhanced through attaching oligoether appendages to a benzyl substituent on imidazole- or aminopyridine-based active units, presumably because of stabilizing n-cation interactions of the ethereal oxygens with the positively charged aza-heterocycle in the catalytic intermediates, and was substantially higher than that of known benchmark catalysts for a range of substrates. Density functional theory calculations and the study of analogues having a lower potential for such stabilizing interactions support our hypothesis.

Beyond PCBM: Methoxylated 1,4-bisbenzyl[60]fullerene adducts for efficient organic solar cells

Organic solar cells have been based mostly on conjugated polymers and the classic fullerene derivative PCBM and are characterized by modest open circuit voltages (Voc). Increasing Voc requires fullerene acceptors with higher LUMOs th

Oxime O-ether compounds and fungicides for agricultural and horticultural use

The present invention relates to novel oxime O-ether compounds represented by a general formula [I]; wherein R1represents C1-6alkyl, C3-6cycloalkyl, C1-6alkoxy, etc., m represents an integer of 1 to 4, R2/

Tetra- and hexa-hydropyrrolo(1,2-a)quinoxaline and azaquinoxaline derivatives

Tetra- and hexa-hydropyrrolo[1,2-a]quinoxaline and azaquinoxaline derivatives of the formula: STR1 in which X is O or H2 ; Y is CH or N; R is hydrogen, alkyl, dialkylaminoalkyl, arylalkyl, phenoxyalkyl, benzoyl, pyridylalkyl or variations there