1027236-70-9

Basic information

• Product Name: Methanesulfonic acid 2-[2-(3-tetradecyloxy-phenyl)-acetylamino]-benzyl ester
• Synonyms: Methanesulfonic acid 2-[2-(3-tetradecyloxy-phenyl)-acetylamino]-benzyl ester
• CAS NO: 1027236-70-9
• Molecular Weight: 531.757
• Mol File: 1027236-70-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Methanesulfonic acid 2-[2-(3-tetradecyloxy-phenyl)-acetylamino]-benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Methanesulfonic acid 2-[2-(3-tetradecyloxy-phenyl)-acetylamino]-benzyl ester(1027236-70-9)
• EPA Substance Registry System: Methanesulfonic acid 2-[2-(3-tetradecyloxy-phenyl)-acetylamino]-benzyl ester(1027236-70-9)

Safety Data

• Hazardous Substances Data: 1027236-70-9(Hazardous Substances Data)

Upstream product

• 124-63-0 methanesulfonyl chloride 
• 138830-36-1 N-[2-(Hydroxymethyl)phenyl]-3-(tetradecyloxy)-benzeneacetamide 
• 5344-90-1 2-Aminobenzyl alcohol 
• 112-71-0 1-Bromotetradecane 
• 42058-59-3 3-hydroxy-benzeneacetic acid, methyl ester 
• 138830-32-7 m-tetradecyloxyphenylacetic acid 
• 138830-33-8 3-(tetradecyloxy)benzeneacetyl chloride 
• 138830-31-6 3-(tetradecyloxy)benzeneacetic acid, methyl ester 

Relevant articles and documents

Analogues of platelet activating factor. 7. Bis-aryl amide and bis-aryl urea receptor antagonists of PAF

A series of bis-aryl amide (13-57 and 66-81) and bis-aryl urea (58 and 85) antagonists of platelet-activating factor (PAF) was prepared that contain, separating the two aromatic rings, linear amide linkages of the form - (CH2)(n)CONH- (n = 0-2), -OCH2CONH-, and -(CH2)(n)NHCO- (n = 0-1), branched amide linkages of the form -(CH2)(n)N(COR)- (n = 1-3, R = CH3 or n-C3H7), and -N(COCH3)CH2-, and urea linkages of the form -NHCONH- and - CH2N(CONHCH3)-. These compounds were examined for their ability to inhibit PAF-induced platelet aggregation of rabbit platelets. These in vitro data were compared to similar data obtained for a number of known PAF antagonists. The compounds were evaluated in vivo, in the mouse, for their ability to prevent death induced by a lethal challenge of PAF. The relationships between the biological activity and the nature, lipophilicity, and position of substituents of the aromatic rings were studied. Best activity was observed for compounds having linkages of the type -CH2CONH-, -CH2N(COR)-, and - CH2NHCO-. Many of these compounds inhibit PAF-induced platelet aggregation with IC50's under 1 μM.