53872-62-1

Basic information

• Product Name: ENONE-C
• Synonyms: ENONE-C;(3aR,4R,5R,6aS)-4-[(1E)-4-(3-Chlorophenoxy)-3-oxo-1-buten-1-yl]hexahydro-5-hydroxy-2H-cyclopenta[b]furan-2-one
• CAS NO: 53872-62-1
• Molecular Formula: C₁₇H₁₇ClO₅
• Molecular Weight: 336.769
• Mol File: 53872-62-1.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 537.84°C at 760 mmHg
• Flash Point: 279.076°C
• Appearance: /
• Density: 1.418
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.637
• CAS DataBase Reference: ENONE-C(CAS DataBase Reference)
• NIST Chemistry Reference: ENONE-C(53872-62-1)
• EPA Substance Registry System: ENONE-C(53872-62-1)

Safety Data

• Hazardous Substances Data: 53872-62-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C17H17ClO5/c18-10-2-1-3-12(6-10)22-9-11(19)4-5-13-14-7-17(21)23-16(14)8-15(13)20/h1-6,13-16,20H,7-9H2/b5-4+/t13-,14-,15-,16+/m1/s1

Upstream product

• 123989-25-3 (1SR,2RS,6SR,8RS)-10-(3-chlorophenoxymethyl)-10,12-dimethoxy-5,9-dioxatricyclo<6.4.0.0^2,6>dodecan-4-one 
• 62515-35-9 (1SR,5RS,6RS,7RS)-6-<4-(3-chlorophenoxy)-3-oxobut-1(E)-en-1-yl>-7-trimethylsiloxy-2-oxabicyclo<3.3.0>octan-3-one 
• 40665-94-9 dimethyl 3-(3-chlorophenoxy)-2-oxopropylphosphonate 
• 62961-72-2 Corey aldehyde 
• 32233-40-2 (3aR,4S,5R,6aS)-5-hydroxy-4-(hydroxymethyl)hexahydro-2H-cyclopenta[b]furan-2-one 
• 26054-46-6 (-)-(1S,5R)-2-oxabicyclo[3.3.0]oct-6-en-3-one 
• 130325-32-5 Formic acid (3aR,4S,5R,6aS)-4-formyloxymethyl-2-oxo-hexahydro-cyclopenta[b]furan-5-yl ester 

Downstream Products

• 40665-92-7 cloprostenol 
• 40665-92-7 16-(m-chlorophenoxy)-9α,11α,15β-trihydroxy-17,18,19,20-tetranor-5-cis-13-trans-prostadienoic acid 
• 52267-81-9 <3aα,4α,5β,6aα>-(+/-)-hexahydro-5-hydroxy-4-<(E)-4-(3-chlorophenoxy)-(3α)-hydroxy-1-butenyl>-2H-cyclopentafuran-2-one 
• 130184-37-1 (3aα,3bβ,6R*,7aα,8aα)-4-(4-(3-chlorophenoxy)-3-oxobutyl)-5-hydroxyhexahydro-2H-cyclopenta[b]furan-2-one 
• 52267-81-9 (3aR,4R,5R,6aS)-4-[(E)-4-(3-Chloro-phenoxy)-3-hydroxy-but-1-enyl]-5-hydroxy-hexahydro-cyclopenta[b]furan-2-one 
• 54276-21-0 (+)-cloprostenol 
• 89560-44-1 (3aR,4R,5R,6aS)-4-[(E)-4-(3-Chloro-phenoxy)-3-hydroxy-but-1-enyl]-hexahydro-cyclopenta[b]furan-2,5-diol 
• 56687-85-5 methyl (8R,9S,11R,12S,15S)-16-(m-chlorophenoxy)-9,11,15-trihydroxy-17,18,19,20-tetranor-5Z,13E-prostadienoate 
• 206555-98-8 cloprostenol 

Relevant articles and documents

Synthesizing method of optical pure cloprostenol

The invention relates to the technical field of medicine preparation, in particular to a synthesizing method of optical pure cloprostenol. The synthesizing method comprises the steps: levogyration corey lactone diol is adopted as a raw material and subjec

Intramolecular Acetalization of 5-Hydroxy Ketones and Enones. A Novel Transformation of Important Prostaglandin Intermediates under Acidic Conditions

Intermediates in the synthesis of ω-tetranor 16-aryloxy prostaglandins, which are 5-hydroxy enones undergo quantitative intramolecular transformation into cyclic methyl acetals in acidic methanolic solution.The reaction proceeds via the corresponding 5-hydroxy-3-methoxy ketones, which partly exist as hemiacetals.The structure of the compounds investigated was elucidated by 1H NMR spectroscopy and by X-ray analysis of the acetal (11).