1344718-97-3

Usage

Physical State

Colorless liquid

Odor

Sweet, floral

Uses

+ Fragrance industry (scent additive)
+ Flavoring agent in food products
+ Intermediate in the synthesis of various organic compounds

Safety Precautions

+ Causes irritation to eyes, skin, and respiratory system upon contact
+ Harmful if ingested or inhaled in large quantities

Upstream product

• 13670-99-0 2,6-difluoroacetophenone 
• 1344718-96-2 1,3-difluoro-2-(1-methoxyprop-1-en-2-yl)benzene 

Downstream Products

• 1344718-99-5 methyl 4-(2,6-difluorophenyl)pent-2-ynoate 
• 1344719-04-5 2-(N-(4-methoxybenzyl)-N-methylamino)-6-(1-(2,6-difluorophenyl)ethyl)pyrimidin-4(3H)-one 
• 1344719-08-9 3-(4-methoxybenzyl)-2-amino-6-(1-(2,6-difluorophenyl)ethyl)pyrimidin-4(3H)-one 
• 1344719-06-7 2-(4-methoxybenzylamino)-6-(1-(2,6-difluorophenyl)ethyl)pyrimidin-4(3H)-one 
• 1344718-98-4 C₁₀H₈Br₂F₂ 

Relevant academic research and scientific papers

Synthesis, Biological Activity, and ADME Properties of Novel S-DABOs/N-DABOs as HIV Reverse Transcriptase Inhibitors

Previous studies aimed at exploring the SAR of C2-functionalized S-DABOs demonstrated that the substituent at this position plays a key role in the inhibition of both wild-type RT and drug-resistant enzymes, particularly the K103N mutant form. The introdu

A domino microwave-assisted protocol for the synthesis of 2,6-disubstituted pyrimidinones

A practical microwave-assisted protocol for the synthesis of 2,6-disubstituted pyrimidinones has been developed. This approach is based on a domino Michael addition-cyclocondensation reaction between substituted thioureas/guanidines and acetylenecarboxyla