144256-13-3

Upstream product

• 120743-99-9 p-[(tert-butyldimethylsilyl)oxy]benzaldehyde 
• 347377-08-6 tert-butyl(4-(2,2-dibromoethenyl)phenoxy)dimethylsilane 
• 123-08-0 4-hydroxy-benzaldehyde 
• 123-11-5 4-methoxy-benzaldehyde 
• 558-13-4 carbon tetrabromide 
• 60512-57-4 1-(2,2-dibromovinyl)-4-methoxybenzene 

Downstream Products

• 1361392-48-4 (E)-4-(2,2-dibromovinyl)phenyl 3-(4-bromophenyl)acrylate 
• 1361392-45-1 4-(2,2-dibromovinyl)phenyl 4-methylbenzoate 
• 1569438-34-1 (Z)-3-bromo-5-(3,5-dichloro-4-hydroxybenzylidene)-4-isopropylfuran-2(5H)-one 
• 1569438-60-3 2,6-dichloro-4-(2,2-dibromovinyl)phenol 
• 1569438-49-8 2,6-dichloro-4-ethynylphenol 
• 2200-91-1 4-ethynylphenol 
• 1394236-51-1 1-(4-(4-(3-chloro-4-(2,5,8,11-tetraoxatridecan-13-yloxy)benzoyloxy)benzoyloxy)phenylmethyl)-4-(4-(4-tetradecyloxybenzoyloxy)phenyl)-1H-1,2,3-triazole 
• 1394236-48-6 1-(4-(4-(3-chloro-4-tetradecyloxybenzoyloxy)benzoyloxy)phenylmethyl)-4-(4-(4-tetradecyloxybenzoyloxy)phenyl)-1H-1,2,3-triazole 
• 1394236-47-5 1-(4-(4-(3-chloro-4-tetradecyloxybenzoyloxy)benzoyloxy)phenylmethyl)-4-(4-(4-(4-tetradecyloxybenzoyloxy)benzoyloxy)phenyl)-1H-1,2,3-triazole 
• 1394236-45-3 1-(4-(4-tetradecyloxybenzoyloxy)phenylmethyl)-4-(4-(4-tetradecyloxybenzoyloxy)phenyl)-1H-1,2,3-triazole 
• 1394236-43-1 1-(4-(4-(4-tetradecyloxybenzoyloxy)benzoyloxy)phenylmethyl)-4-(4-(4-tetradecyloxybenzoyloxy)phenyl)-1H-1,2,3-triazole 
• 1394236-41-9 1-(4-(4-tetradecyloxybenzoyloxy)phenylmethyl)-4-(4-(4-(4-tetradecyloxybenzoyloxy)benzoyloxy)phenyl)-1H-1,2,3-triazole 
• 1394236-39-5 1-(4-(4-(4-tetradecyloxybenzoyloxy)benzoyloxy)phenylmethyl)-4-(4-(4-(4-tetradecyloxybenzoyloxy)benzoyloxy)phenyl)-1H-1,2,3-triazole 
• 1394236-37-3 1-(4-(4-tetradecyloxybenzoyloxy)phenyl)-4-(4-(4-tetradecyloxybenzoyloxy)phenyl)-1H-1,2,3-triazol 

Relevant academic research and scientific papers

Copper-catalyzed domino route to natural nostoclides and analogues: A total synthesis of nostoclides i and II

An original and convenient domino route to natural nostoclides I and II has been developed using a two-step sequence consisting of a copper-cat-alyzed tandem reaction associated with Suzuki cross-coupling. The methodology employed for this total synthesis appeared to be an interesting and suffi-ciently flexible tool to allow the synthesis of numer-ous analogues of these nostoclides.

Synthesis of 4-(2,2-dibromovinyl)phenol and its one-pot esterification

In situ treatment of 4-(2,2-dibromovinyl)phenol, which was prepared from 4-hydroxybenzaldehyde and carbon tetrabromide in CH2Cl2 under Corey-Fuchs conditions, with a diverse range of acids in the presence of dicyclohexyl-carbodiimide

"Click chemistry" as a versatile route to synthesize and modulate bent-core liquid crystalline materials

Three series of bent-shaped compounds containing the 1,2,3-triazole ring in the central core of the molecule have been prepared by the most extended "click chemistry" reaction, the copper-catalyzed azide-alkyne cycloaddition (CuAAC). This research demonstrates the versatility of this synthetic approach with the aim of achieving innovative compact supramolecular organizations. The appropriate combination of the 1,2,3-triazole synthon linked either to a methylene unit (series M) or to a methylenoxycarbonyl block (series MC) has allowed the induction of a variety of non-classical bent-core liquid crystal phases versus the classic mesophases promoted by 1,4-diphenyl-1,2,3- triazole derivatives (series T). Through a suitable selection of common lateral structures connected by "click chemistry" both the transition temperatures and mesomorphism, ranging from lamellar to columnar or B4-like supramolecular liquid crystalline organizations, can be tuned. The Royal Society of Chemistry 2012.

METHOXYIMINO COMPOUNDS AND FUNGICIDE COMPOSITION COMPRISING SAME

The present invention provides a methoxyimino compound, and a fungicide composition comprising same as an active ingredient. The methoxyimino compound of the present invention, which has an excellent antifungal activity against a wide spectrum of fungi even at a low application rate, can be used to protect various crops.

3α-Hydroxy-3β-(phenylethynyl)-5β-pregnan-20-ones: Synthesis and pharmacological activity of neuroactive steroids with high affinity for GABA(A) receptors

Neuroactive steroids that allosterically modulate GABA(A) receptors have potential uses as anticonvulsants, anxiolytics, and sedative-hypnotic agents. Recently, a series of pregnanes substituted with simple alkyl groups at the 3β-position were synthesized

Development of a highly cardioselective ultra short-acting β-blocker, ONO-1101

A novel, highly cardioselective ultra short-acting β-blocker, ONO-1101, has been developed for application in the emergency treatment of tachycardia and better control of heart rate in surgery. This agent is approximately nine times more potent in β-blocking activity in vivo and eight times more cardioselective in vitro than esmolol. This β-blocking drug has a short duration of activity, enabling rapid recovery after cessation of administration if side effects occur. It can be used safely in patients suffering from acute heart disease and represents a major therapeutic advance in the treatment of heart disease.