790187-59-6

Basic information

• Product Name: 2-[({5-(2,6-dimethoxyphenyl)-1-[4-({[3-(dimethylamino)propyl]amino}carbonyl)-2-isopropylphenyl]-1H-pyrazol-3-yl}carbonyl)amino]adamantane-2-carboxylic acid
• Synonyms: 2-[({5-(2,6-dimethoxyphenyl)-1-[4-({[3-(dimethylamino)propyl]amino}carbonyl)-2-isopropylphenyl]-1H-pyrazol-3-yl}carbonyl)amino]adamantane-2-carboxylic acid
• CAS NO: 790187-59-6
• Molecular Weight: 671.837
• Mol File: 790187-59-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-[({5-(2,6-dimethoxyphenyl)-1-[4-({[3-(dimethylamino)propyl]amino}carbonyl)-2-isopropylphenyl]-1H-pyrazol-3-yl}carbonyl)amino]adamantane-2-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[({5-(2,6-dimethoxyphenyl)-1-[4-({[3-(dimethylamino)propyl]amino}carbonyl)-2-isopropylphenyl]-1H-pyrazol-3-yl}carbonyl)amino]adamantane-2-carboxylic acid(790187-59-6)
• EPA Substance Registry System: 2-[({5-(2,6-dimethoxyphenyl)-1-[4-({[3-(dimethylamino)propyl]amino}carbonyl)-2-isopropylphenyl]-1H-pyrazol-3-yl}carbonyl)amino]adamantane-2-carboxylic acid(790187-59-6)

Safety Data

• Hazardous Substances Data: 790187-59-6(Hazardous Substances Data)

Upstream product

• 81090-34-8 4-bromo-2-isopropyl-aniline 
• 1476068-47-9 methyl 1-(4-bromo-2-isopropylphenyl)-5-(2,6-dimethoxyphenyl)-1H-pyrazole-3-carboxylate 
• 643-28-7 2-isopropylaniline 
• 50294-51-4 2-(amino)tricyclo[3.3.1.13,7]decane-2-carboxylic acid hydrochloride 
• 1476064-46-6 2-({[1-(4-bromo-2-isopropylphenyl)-5-(2,6-dimethoxyphenyl)-1H-pyrazole-3-yl]carbonyl}amino)adamantane-2-carboxylic acid 
• 109-55-7 1-amino-3-(dimethylamino)propane 
• 13939-06-5 molybdenum hexacarbonyl 
• 1279881-34-3 1-(4-bromo-2-isopropylphenyl)-5-(2,6-dimethoxyphenyl)-1H-pyrazole-3-carboxylic acid 

Relevant articles and documents

Efficient synthesis of heterocyclic neurotensin receptor ligands by microwave-assisted aminocarbonylation

Marking the heterocyclic neurotensin receptor antagonist SR142948A as a lead compound, the development of an efficient and a practical synthetic route to heterocyclic aryl carboxamides is reported. Thus, a highly efficient and flexible access to these carboxamides was elaborated by taking advantage of microwave-assisted aminocarbonylation reaction mediated by Mo(CO)6, Herrmann's palladacycle, [(t-Bu)3PH]BF4, and DBU.