57641-21-1

Basic information

• Product Name: 1,3-Diphenoxyacetone
• Synonyms: 1,3-Diphenoxyacetone
• CAS NO: 57641-21-1
• Molecular Weight: 242.274
• Mol File: 57641-21-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1,3-Diphenoxyacetone(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Diphenoxyacetone(57641-21-1)
• EPA Substance Registry System: 1,3-Diphenoxyacetone(57641-21-1)

Safety Data

• Hazardous Substances Data: 57641-21-1(Hazardous Substances Data)

Upstream product

• 622-04-8 1,3-diphenoxy-2-propanol 
• 816-39-7 1,3-dibromoroacetone 
• 119-36-8 methyl salicylate 
• 108-95-2 phenol 
• 701-99-5 Phenoxyacetyl chloride 
• 36304-22-0 tert-butyl 2-phenoxyacetate 
• 66535-70-4 2-Trimethylsiloxy-1.3-diphenoxypropan 

Downstream Products

• 1196475-98-5 C₂₈H₂₄O₄S 
• 1196475-97-4 C₂₇H₂₀BrNO₂S 
• 170124-04-6 4-(Dimethylamino)-1,3-diphenoxy-3-buten-2-one 
• 170124-05-7 4-(Butylthio)-1,3-diphenoxy-3-buten-2-one 

Relevant articles and documents

An economical noncatalytic approach to the synthesis of congested diaryl ethers and aryl benzyl thioethers through C-C insertion

An efficient one-pot synthesis of diaryl ethers and aryl benzyl thioethers has been delineated through base-induced ring transformation of 6-aryl-4-methylthio-2H-pyran-2-one-3-carbonitriles, methyl 6-aryl-4-methylthio- 2H-pyran-2-one-3-carboxylates and 6-aryl-4-(piperidin-1-yl)-2H-pyran-2-one-3- carbonitriles by either 1-phenoxypropan-2-one, 1,3-diphenoxypropan-2-one or 4-arylthiobutan-2-one, under very mild reaction conditions, in excellent yield. Georg Thieme Verlag Stuttgart.

CYSTEINE PROTEASE INHIBITORS EFFECTIVE FOR IN VIVO USE

A method of treating medical conditions with proteinase inhibitors of the formula: STR1 wherein B is H or an amino acid blocking group for the N-terminal amino acid nitrogen;R. sub.1 is an optionally protected α-amino acid side chain such that P. su

A novel reaction for the functionalization of epoxy resins: New regio- and chemoselective ring-opening of epoxides with aryl silyl ether catalyzed by cesium fluoride

By use of cesium fluoride as a catalyst, aryl or alkyl glycidyl ethers were ring-opened by aryl trimethylsilyl ether to produce O-protected aryloxyhydrins with a quantitative regioselectivity for the first time. Alkyl silyl ether was ineffective for this ring-opening.