反応式
C[C:2]12[CH2:11][CH2:10][CH2:9][CH2:8][CH:7]1[C:6](=[O:12])[O:5][C:3]2=[O:4].C(C1CC(=O)OC1=O)=CCCCCCCCCCC.CC#C>>[C:6]1(=[O:12])[O:5][C:3](=[O:4])[C:2]2=[CH:11][CH:10]=[CH:9][CH:8]=[C:7]12参加物
4
実験手順
The procedures of Example 1 were repeated except that 38.2 g. of methylhexahydrophthalic anhydride (Example 2) and 61.2 g. of dodecenylsuccinic anhydride (Example 3) which was a maleinization product of propylene tetramer or butylene trimer, were employed, respectively, instead of 34 g. of phthalic anhydride, to give light yellow resins. The properties thereof are shown in Table 1.
出典と根拠
- ORDレコード
- ord-bf0250d297b14922ad23662d06f7e4b0
- 出典データセット
- uspto-grants-1985_03
- 特許番号
- US04507376
関連ノート
読み込み中…