176208-16-5

Upstream product

• 4746-97-8 cyclohexanedione monoethylene ketal 
• 623-00-7 4-bromobenzenecarbonitrile 
• 163260-71-7 4-(1,4-dioxaspiro[4.5]dec-7-en-8-yl)benzoic acid 
• 74-88-4 methyl iodide 
• 680596-79-6 4,4,5,5-tetramethyl-2-(1,4-dioxaspiro[4.5]dec-7-en-8-yl)-1,3,2-dioxaborolane 
• 619-42-1 4-methoxycarbonylphenyl bromide 
• 99768-12-4 4-methoxycarbonylphenylboronic acid 
• 170011-47-9 1,4-dioxaspiro[4.5]dec-7-en-8-yl trifluoromethanesulfonate 
• 139504-91-9 4-(4-carbomethoxyphenyl)-4-hydroxycyclohexanone 
• 137464-97-2 4-(4'-carbomethoxyphenyl)-4-hydroxycyclohexanone ethylene ketal 

Downstream Products

• 176208-17-6 methyl 4-<4-<(2-amino-4(3H)-oxopyrimidin-6-yl)hydrazono>cyclohexyl>benzoate 
• 176208-18-7 methyl 4-(2-amino-3,5,6,7,8,9-hexahydro-4-oxo-4H-pyrimido<4,5-b>indol-6-yl)benzoate 
• 176208-19-8 4-(2-amino-3,5,6,7,8,9-hexahydro-4-oxo-4H-pyrimido<4,5-b>indol-6-yl)benzoic acid 
• 137464-98-3 4-(4-oxocyclohexyl)benzoic acid methyl ester 
• 885706-16-1 methyl 4-(1,4-dioxaspiro[4.5]decan-8-yl)benzoate 

Relevant academic research and scientific papers

NOVEL ORGANIC COMPOUND, NEAR-INFRARED FLUORESCENT CONSTANT MEDIUM CONTAINING SAME, AND METHOD FOR NANO-GRANULATING CONSTANT MEDIUM

The present invention relates to a novel organic compound, a near-infrared fluorescent constant medium containing the same, and a method for nano-granulating the constant medium.

Overcoming hERG activity in the discovery of a series of 4-azetidinyl-1-aryl-cyclohexanes as CCR2 antagonists

A series of 4-azetidinyl-1-aryl-cyclohexanes as potent CCR2 antagonists with high selectivity over activity for the hERG potassium channel is discovered through divergent SARs of CCR2 and hERG.

2-(ARYL)AZACYCLYLMETHYL CARBOXYLATES, SULFONATES, PHOSPHONATES, PHOSPHINATES AND HETEROCYCLES AS S1P RECEPTOR AGONISTS

The present invention encompasses compounds of Formula I: as well as the pharmaceutically acceptable salts thereof. The compounds are S1P1/Edg1 receptor agonists and thus have immunosuppressive, anti-inflammatory and hemostatic activities by mo

A fischer-indole approach to pyrrolo[2,3-d]pyrimidines

Several new 5,6-disubstituted pyrrolo[2,3-d]pyrimidines have been prepared by thermolysis of ketone hydrazones of 2-amino-6-hydrazino4(3H)-oxopyrimidine (8) (the Fischer-Indole Synthesis).