110451-90-6

Upstream product

• 108-68-9 3,5-Dimethylphenol 
• 164513-49-9 2-bromo-1-(bromomethyl)-5-methoxy-3-methylbenzene 
• 6267-34-1 2-bromo-5-methoxy-1,3-dimethyl-benzene 
• 874-63-5 3,5-dimethylmethoxybenzene 
• 94742-92-4 methyl 2-bromo-5-methoxy-3-methylbenzoate 

Downstream Products

• 174417-54-0 2-bromo-5-methoxy-3-methylbenzoic acid 
• 202195-07-1 3-methoxy-5-methyl-2-(1,4,5-trimethoxynaphthalen-2-yl)benzaldehyde 
• 199612-65-2 2-iodo-3-methoxy-5-methylbenzaldehyde 
• 119650-45-2 (2-iodo-3-methoxy-5-methylphenyl)methanol 
• 119650-44-1 (3-methoxy-5-methylphenyl)methanol 
• 7414-92-8 Tetrangulol 
• 1362209-16-2 2-bromo-5-methoxy-1-methyl-3-vinylbenzene 
• 1308649-72-0 2-bromo-5-methoxy-3-methylbenzaldehyde 
• 207287-39-6 (S)-2-(2-Bromo-5-methoxy-3-methyl-phenyl)-4-isopropyl-4,5-dihydro-oxazole 
• 631910-75-3 (2-bromo-5-methoxy-3-methyl-benzyloxy)-acetic acid tert-butyl ester 
• 94742-92-4 methyl 2-bromo-5-methoxy-3-methylbenzoate 

Relevant academic research and scientific papers

New 2,2′-substituted 4,4′-dimethoxy-6,6′-dimethyl[1, 1′-biphenyls], inducing a strong helical twisting power in liquid crystals

Based on the stabilisation of the molecular motion by the chiral residue, novel optically active biphenylic chiral dopants for nematic liquid crystals were developed. This molecular congestion was obtained by introducing mesogenic residues on the 2,2′-positions of the chiral biphenyl; this led to a novel molecular architecture that was found to be efficient. The synthesised optically active biphenyls were characterised with very short cholesteric pitches when used as chiral dopants in nematic liquid crystals. The synthesis of the enatiomerically pure biphenyl dopants and their preliminary physicochemical characterisations are described.

Reactions of [2-(2-Naphthyl)phenyl]acetylenes and 2-(2-Naphthyl)benzaldehyde O-Phenyloximes: Synthesis of the Angucycline Tetrangulol and 1,10,12-Trimethoxy-8-methylbenzo[c]phenanthridine

The Suzuki–Miyaura coupling reaction between (1,4,5-trimethoxynaphthalen-2-yl)boronic acid and 2-iodo-3-methoxy-5-methylbenzaldehyde gave the intermediate 3-methoxy-5-methyl-2-(1,4,5-trimethoxynaphthalen-2-yl)benzaldehyde. Conversion of this benzaldehyde

Novel thiophene amidines, compositions thereof, and methods of treating complement-mediated diseases and conditions

Disclosed is a method for treating the symptoms of an acute or chronic disorder mediated by the classical pathway of the complement cascade, comprising administering to a mammal in need of such treatment a therapeutically effective amount of a compound of Formula I or a solvate, hydrate or pharmaceutically acceptable salt thereof; wherein R1, R2, R3, R4 and R7 are defined in the specification, Z is SO or SO2, and Ar is an aromatic or heteroaromatic group as defined herein.

NOVEL THIOPHENE AMIDINES, COMPOSITIONS THEREOF, AND METHODS OF TREATING COMPLEMENT-MEDIATED DISEASES AND CONDITIONS

Disclosed is a method for treating the symptoms of an acute or chronic disorder mediated by the classical pathway of the complement cascade, comprising administering to a mammal in need of such treatment a therapeutically effective amount of a compound of Formula (I) or a solvate, hydrate or pharmaceutically acceptable salt thereof; wherein R1, R2, R3, R4 and R7 are defined in the specification, Z is SO or SO2, and Ar is an aromatic or heteroaromatic group as defined herein.

A New Family of Enantiomerically Pure Smectic C* Liquid Crystals with a Bridged Chiral Biphenyl Core

The synthesis of enantiomerically pure bridged biphenyl compounds, (-)-(R)-3,9-bis(4-(dodecyloxy)benzoyloxy)-5,7-dihydro-1,11-dimethyldibenzo[c,e] thiepine, 13, and (-)-(R)-3,9-bis(4-(dodecyloxy)benzoyloxy)-5,7-dihydro-1,11-dimethyldibenzo[c,e]- thiepin d

Naturally Occuring Dibenzofurans. Part 9. A Convenient Synthesis of Phthalides: The Synthesis of Methyl Di-O-methylporphyrilate

A convenient synthesis of phthalides from o-halogenobenzyl alcohols is described.This method is then applied to the synthesis of methyl di-O-methylporphyrilate (methyl 1,3-dihydro-4,10-dimethoxy-8-methyl-3-oxoisobenzofuro