146271-57-0

Upstream product

• 439126-19-9 dimethyl 4-amino-5-methylphthalate 
• 32001-55-1 pyridine hydrogenfluoride 
• 167992-81-6 dimethyl 4-methyl-5-nitro-phthalate 
• 19438-61-0 4-methylphthalic anhydride 
• 42760-52-1 4-Methyl-5-nitro-phthalic acid 
• 146271-53-6 2-fluoro-3-methyl-1-(trimethylsilyloxy)buta-1,3-diene 
• 762-42-5 dimethyl acetylenedicarboxylate 

Relevant academic research and scientific papers

Achieving Balanced Charge Transport and Favorable Blend Morphology in Non-Fullerene Solar Cells via Acceptor End Group Modification

Generally, the electron-withdrawing substitution on the end-capping group of the acceptor-donor-acceptor type small-molecule acceptor (SMA) narrows the optical bandgap, and the electron-donating group lifts the lowest unoccupied molecular orbital (LUMO) e

Polysubstituted benzocyclopentadione derivative-based A-D-A conjugated molecule and application thereof

The invention discloses a polysubstituted benzocyclopentadione derivative-based A-D-A conjugated molecule and application thereof. The application chemical structural general formula of the conjugatedmolecule is as shown in the specification. According to

Inhibitors of papilloma virus

A compound of formula (I) or its enantiomers or diastereoisomers thereof: wherein: A,; X, W, R1, Y; R3; and R4 are as defined herein. The compounds of the invention may be used as inhibitors of the papilloma virus E1-E2-DN

The Diels-Alder approach to musk odor type arenes

The readily accessible 2-halogeno-1-trimethylsilyloxy-1,3-butadienes react smoothly with dimethyl acetylenedicarboxylate to afford 4-halophthalic esters. One of these cycloadducts was subsequently converted into heterocyclic analogues of phantolide like musk fragrances.