1054812-72-4

Basic information

• Product Name: Acetic acid (2R,3R,4S,5R,6S)-4,5-diacetoxy-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-6-[4-(2-nitro-ethyl)-phenoxy]-tetrahydro-pyran-3-yl ester
• CAS NO: 1054812-72-4
• Molecular Weight: 727.765
• Mol File: 1054812-72-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Acetic acid (2R,3R,4S,5R,6S)-4,5-diacetoxy-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-6-[4-(2-nitro-ethyl)-phenoxy]-tetrahydro-pyran-3-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid (2R,3R,4S,5R,6S)-4,5-diacetoxy-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-6-[4-(2-nitro-ethyl)-phenoxy]-tetrahydro-pyran-3-yl ester(1054812-72-4)
• EPA Substance Registry System: Acetic acid (2R,3R,4S,5R,6S)-4,5-diacetoxy-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-6-[4-(2-nitro-ethyl)-phenoxy]-tetrahydro-pyran-3-yl ester(1054812-72-4)

Safety Data

• Hazardous Substances Data: 1054812-72-4(Hazardous Substances Data)

Upstream product

• 74213-97-1 2',3',4',6'-tetra-O-acetylthalicoside 
• 74213-96-0 glucoside de 4-(-2-nitroethyl) phenol 
• 74808-10-9 O-(2,3,4,6-Tetra-O-acetyl-α-D-glucopyranosyl)trichloroacetimidate 
• 37567-58-1 2-(4-hydroxyphenyl)-1-nitroethane 

Downstream Products

• 153042-86-5 Acetic acid (2S,3R,4S,5R,6R)-4,5-diacetoxy-6-hydroxymethyl-2-[4-(2-nitro-ethyl)-phenoxy]-tetrahydro-pyran-3-yl ester 

Relevant articles and documents

Medicinal foodstuffs. II. On the bioactive constituents of the tuber of Sagittaria trifolia L. (Kuwai, Alismataceae): Absolute stereostructures of trifoliones A, B, C, and D, sagittariosides a and b, and arabinothalictoside

From the medicinal foodstuff 'kuwai', the tuber of Sagittaria trifolia L., four bioactive diterpene ketones, trifoliones A, B, C, and D, two diterpene glucosides, sagittariosides a and b, and a nitroethylphenol glycoside, arabinothalictoside, were isolated, together with six known diterpenes. Their absolute stereostructures were determined on the basis of chemical and physicochemical evidence which included the application of a modified Mosher's method and an exciton chirality method. Among the diterpene constituents, trifoliones A, B, C, and D exhibited inhibitory effects on the histamine release from rat mast cells induced by compound 48/80 and calcium ionophore A-23187.