109586-70-1

Basic information

• Product Name: 6-<(2-endo,3-exo)-3-<<2-(3-Methoxyphenyl)ethyl>carbamoyl>bicyclo<2.2.1>hept-2-yl>hexansaeure
• CAS NO: 109586-70-1
• Molecular Weight: 387.519
• Mol File: 109586-70-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 6-<(2-endo,3-exo)-3-<<2-(3-Methoxyphenyl)ethyl>carbamoyl>bicyclo<2.2.1>hept-2-yl>hexansaeure(CAS DataBase Reference)
• NIST Chemistry Reference: 6-<(2-endo,3-exo)-3-<<2-(3-Methoxyphenyl)ethyl>carbamoyl>bicyclo<2.2.1>hept-2-yl>hexansaeure(109586-70-1)
• EPA Substance Registry System: 6-<(2-endo,3-exo)-3-<<2-(3-Methoxyphenyl)ethyl>carbamoyl>bicyclo<2.2.1>hept-2-yl>hexansaeure(109586-70-1)

Safety Data

• Hazardous Substances Data: 109586-70-1(Hazardous Substances Data)

Upstream product

• 100557-75-3 Methyl-6-<(2-endo,3-exo)-3-carboxybicyclo<2.2.1>hept-2-yl>hexanoat 
• 100557-86-6 Methyl-(Z)-6-<(2-endo,3-endo)-3-(hydroxymethyl)bicyclo<2.2.1>hept-5-en-2-yl>-5-hexenoat 
• 100557-86-6 Methyl-(Z)-6-<(2-exo/endo,3-exo)-3-(hydroxymethyl)bicyclo<2.2.1>hept-5-en-2-yl>-5-hexenoat 
• 100557-84-4 (Z)-6-<(2-endo,3-endo)-3-(Hydroxymethyl)bicyclo<2.2.1>hept-5-en-2-yl>-5-hexensaeure 
• 100557-74-2 Methyl-6-<(2-endo,3-endo)-3-(hydroxymethyl)bicyclo<2.2.1>hept-2-yl>-hexanoat 
• 100557-74-2 Methyl-6-<(2-exo/endo,3-exo)-3-(hydroxymethyl)bicyclo<2.2.1>hept-2-yl>hexanoat 
• 100557-82-2 (1α,3aα,4α,7α,7aα)-1,3,3a,4,7,7a-Hexahydro-4,7-methanoisobenzofuran-1-ol 
• 64550-47-6 (3aS*,4R*,7S*,7aR*)-3a,4,7,7a-tetrahydro-4,7-methanoisobenzofuran-1(3H)-one 
• 17814-85-6 (4-carboxybutyl)triphenylphosphonium bromide 
• 109586-67-6 Methyl-6-<(2-endo,3-exo)-3-<<2-(3-methoxyphenyl)ethyl>carbamoyl>bicyclo<2.2.1>hept-2-yl>hexanoat 
• 100557-75-3 Methyl-6-<(2-exo/endo,3-exo)-3-carboxybicyclo<2.2.1>hept-2-yl>hexanoat 
• 2039-54-5 2-(meta-methoxyphenyl)-ethylamine hydrochloride 
• 109586-67-6 Methyl-6-<(2-exo/endo,3-exo)-3-<<2-(3-methoxyphenyl)ethyl>carbamoyl>bicyclo<2.2.1>hept-2-yl>hexanoat 

Relevant articles and documents

6-(3-Carbamoylbicyclohept-2-yl)hexanoic Acids, a New Class of TxA2 Antagonists

The synthesis of prostanoids 20-27, 40a, b, and 45a, b starting from the educts 1a, b, and 31 is described.Configurational changes concerning to the positions 2 and 3 of the bicyclic system were proofed by 13C-NMR spectroscopy and were also used for the preparation of the four exo/endo derivatives. 25 and 26 are potent TxA2 antagonists.