JPS646236A - Di(meth)acrylic acid ester - Google Patents

Di(meth)acrylic acid ester

Info

Publication number
JPS646236A
JPS646236A JP15964187A JP15964187A JPS646236A JP S646236 A JPS646236 A JP S646236A JP 15964187 A JP15964187 A JP 15964187A JP 15964187 A JP15964187 A JP 15964187A JP S646236 A JPS646236 A JP S646236A
Authority
JP
Japan
Prior art keywords
compound
formula
acrylic acid
meth
acid ester
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
Application number
JP15964187A
Other languages
Japanese (ja)
Inventor
Masayuki Kuroki
Minoru Yokoshima
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Kayaku Co Ltd
Original Assignee
Nippon Kayaku Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Nippon Kayaku Co Ltd filed Critical Nippon Kayaku Co Ltd
Priority to JP15964187A priority Critical patent/JPS646236A/en
Publication of JPS646236A publication Critical patent/JPS646236A/en
Pending legal-status Critical Current

Links

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Macromonomer-Based Addition Polymer (AREA)

Abstract

NEW MATERIAL:A di(meth)acrylic acid ester shown by formula I [R1 is 4-10 alkylene; R2 is H or CH3; average value of (a) and (b) are 0-5, respectively and average total value of a+b is 0.5-5 number; average value of l is 1-20]. USE:Useful as a vehicle for printing ink and coating compounds. Liquid at normal temperature and readily handleable. A coating film obtained by the compound has excellent flexing properties. The compound has improved curing properties. PREPARATION:A carbonate diol shown by formula II is reacted with acrylic acid or methacrylic acid under heating preferably pressure a polymerization inhibitor such as hydroquinone at 50 deg.C-130 deg.C, preferably 65 deg.C-90 deg.C to give a compound shown by formula I. The compound shown by formula II, for example, is synthesized by subjecting an adduct of beta-methyl-delta-valerolactone with a diol compound and a diacryl carbonate to ester interchange reaction.
JP15964187A 1987-06-29 1987-06-29 Di(meth)acrylic acid ester Pending JPS646236A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15964187A JPS646236A (en) 1987-06-29 1987-06-29 Di(meth)acrylic acid ester

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15964187A JPS646236A (en) 1987-06-29 1987-06-29 Di(meth)acrylic acid ester

Publications (1)

Publication Number Publication Date
JPS646236A true JPS646236A (en) 1989-01-10

Family

ID=15698152

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15964187A Pending JPS646236A (en) 1987-06-29 1987-06-29 Di(meth)acrylic acid ester

Country Status (1)

Country Link
JP (1) JPS646236A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5354369A (en) * 1992-05-13 1994-10-11 Canon Kabushiki Kaisha Ink, ink-jet recording process making use of the ink, and equipment therefor

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5354369A (en) * 1992-05-13 1994-10-11 Canon Kabushiki Kaisha Ink, ink-jet recording process making use of the ink, and equipment therefor

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