JPS6475447A - Phenanthrene compound - Google Patents
Phenanthrene compoundInfo
- Publication number
- JPS6475447A JPS6475447A JP23414087A JP23414087A JPS6475447A JP S6475447 A JPS6475447 A JP S6475447A JP 23414087 A JP23414087 A JP 23414087A JP 23414087 A JP23414087 A JP 23414087A JP S6475447 A JPS6475447 A JP S6475447A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- expressed
- compound
- phenanthrene
- compound expressed
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Landscapes
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polymerisation Methods In General (AREA)
Abstract
NEW MATERIAL:A phenanthrene compound, expressed by formula I [A is formula II (n is an integer of >=1); R1 is OH or formula III; R2 is H or CH3] and having polymerizability. EXAMPLE:2,7-Diphenanthryldiglycidyl methacrylate expressed by formula I (R1 is OH; R2 is CH3). USE:A resin raw material curable by light or electron rays, having excellent adhesive properties to metal, paper, etc., hardness and heat resistance and useful as coatings, inks, adhesives, hard coats, presensitized (PS) plates, resins for composite materials or heat-resistant resins. PREPARATION:Phenanthrene expressed by formula IV is hydrogenated to form 9,10-dihydrophenanthrene expressed by formula V, which is then iodinated to provide a compound expressed by formula VI. The resultant compound expressed by formula VI is subsequently hydrolyzed to form a compound expressed by formula VII, which is then epoxidized with epichlorohydrin and reacted with methacrylic acid in a molar amount of twice based on the resultant epoxy compound to afford the aimed compound expressed by formula I (R1 is OH and R2 is CH3).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP23414087A JPS6475447A (en) | 1987-09-18 | 1987-09-18 | Phenanthrene compound |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP23414087A JPS6475447A (en) | 1987-09-18 | 1987-09-18 | Phenanthrene compound |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS6475447A true JPS6475447A (en) | 1989-03-22 |
Family
ID=16966269
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP23414087A Pending JPS6475447A (en) | 1987-09-18 | 1987-09-18 | Phenanthrene compound |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6475447A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010254585A (en) * | 2009-04-22 | 2010-11-11 | Kawasaki Kasei Chem Ltd | Anthracene-9,10-diether compound, method for producing the same and polymer thereof |
| JP2016504433A (en) * | 2012-11-21 | 2016-02-12 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングＭｅｒｃｋ Ｐａｔｅｎｔ Ｇｅｓｅｌｌｓｃｈａｆｔ ｍｉｔ ｂｅｓｃｈｒａｅｎｋｔｅｒ Ｈａｆｔｕｎｇ | Polymerizable compounds and their use in liquid crystal displays |
-
1987
- 1987-09-18 JP JP23414087A patent/JPS6475447A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010254585A (en) * | 2009-04-22 | 2010-11-11 | Kawasaki Kasei Chem Ltd | Anthracene-9,10-diether compound, method for producing the same and polymer thereof |
| JP2016504433A (en) * | 2012-11-21 | 2016-02-12 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングＭｅｒｃｋ Ｐａｔｅｎｔ Ｇｅｓｅｌｌｓｃｈａｆｔ ｍｉｔ ｂｅｓｃｈｒａｅｎｋｔｅｒ Ｈａｆｔｕｎｇ | Polymerizable compounds and their use in liquid crystal displays |
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