13318-11-1

Basic information

• Product Name: Oxiranemethanol, 4-nitrobenzoate
• CAS NO: 13318-11-1
• Molecular Formula: C10H9NO5
• Molecular Weight: 223.185
• Mol File: 13318-11-1.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Oxiranemethanol, 4-nitrobenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: Oxiranemethanol, 4-nitrobenzoate(13318-11-1)
• EPA Substance Registry System: Oxiranemethanol, 4-nitrobenzoate(13318-11-1)

Safety Data

• Hazardous Substances Data: 13318-11-1(Hazardous Substances Data)

Upstream product

• 619-50-1 4-nitrobenzoic acid methyl ester 
• 556-52-5 oxiranyl-methanol 
• 3847-57-2 sodium 4-nitrobenzoate 
• 106-89-8 epichlorohydrin 
• 62-23-7 4-nitro-benzoic acid 
• 122-04-3 4-nitro-benzoyl chloride 

Downstream Products

• 115231-11-3 2-O-(4-nitrobenzoyl)glycerol 
• 851768-17-7 2-O-(4-nitrobenzoyl)-1,3-bis-O-(trifluoroacetyl)glycerol 
• 292601-63-9 Glycidyl 4-aminobenzoate 
• 106268-95-5 (R)-glycidyl 4-nitrobenzoate 
• 60456-23-7 (S)-oxiranemethanol 
• 106269-07-2 3-(phenylyhio)-1,2-propanediol 2-O-p-nitrobenzoate 
• 106269-06-1 3-(phenylyhio)-1,2-propanediol 1-O-p-nitrobenzoate 
• 5149-48-4 3-(phenylthio)-1,2-propanediol 
• 106356-60-9 3-cyano-1,2-propanediol 1-O-p-nitrobenzoate 
• 27913-70-8 glycerol mono-p-nitrobenzoate 

Relevant articles and documents

A convenient preparation of di-p-chlorobenzyl azodicarboxylate (DCAD) for mitsunobu couplings

Gram-scale synthesis of pure, bench-stable solid di-p-chlorobenzyl azodicarboxylate (DCAD) is performed in two steps without resorting to chromatography. This novel reagent effects Mitsunobu couplings with yields comparable to DEAD or DIAD, while addressi

METHOD FOR PRODUCING GLYCIDYL ESTER

PROBLEM TO BE SOLVED: To provide a production method which makes it possible to obtain glycidyl ester with high yields from the ester exchange reaction between ester and glycidol with a convenient catalyst in a mild reaction condition. SOLUTION: Glycidyl ester is produced by the ester exchange reaction between ester and glycidol in the presence of a polystyrene-carrying quaternary ammonium salt. SELECTED DRAWING: None COPYRIGHT: (C)2017,JPOandINPIT

Regioselective opening of an oxirane system with trifluoroacetic anhydride. A general method for the synthesis of 2-monoacyl- and 1,3-symmetrical triacylglycerols

A trifluoroacetic anhydride-catalyzed opening of the oxirane system of glycidyl esters with a simultaneous migration of the acyl group provides a new, efficient entry to either 2-monoacylglycerols (2-MAG) or 1,3-symmetrical triglycerides (1,3-STG) as potential prodrug frameworks.