BE1005299A3

BE1005299A3 - Bis-(benzofuranne-2-ones) et leur application a la stabilisation de matieres organiques.

Bis-(benzofuranne-2-ones) et leur application a la stabilisation de matieres organiques. Download PDF

Info

Publication number: BE1005299A3
Authority: BE; Belgium
Prior art keywords: sep; butyl; bis; tert; hydroxy
Prior art date: 1991-07-01

Application number

BE9200595A

Other languages

English (en)

French (fr)

Original Assignee

Ciba Geigy Ag

Priority date

1991-07-01

Filing date

1992-06-25

Publication date

1993-06-22

1992-06-25 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1993-06-22 Application granted granted Critical

1993-06-22 Publication of BE1005299A3 publication Critical patent/BE1005299A3/fr

Links

ACZGCWSMSTYWDQ-UHFFFAOYSA-N 3h-1-benzofuran-2-one Chemical class C1=CC=C2OC(=O)CC2=C1 ACZGCWSMSTYWDQ-UHFFFAOYSA-N 0.000 title abstract description 5
230000006641 stabilisation Effects 0.000 title description 11
238000011105 stabilization Methods 0.000 title description 11
239000011368 organic material Substances 0.000 title description 6
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 19
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 18
239000001257 hydrogen Substances 0.000 claims abstract description 17
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 13
125000003884 phenylalkyl group Chemical group 0.000 claims abstract description 4
125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 3
150000001875 compounds Chemical class 0.000 claims description 66
150000003254 radicals Chemical class 0.000 claims description 19
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
150000002431 hydrogen Chemical class 0.000 claims description 8
125000004423 acyloxy group Chemical group 0.000 claims description 7
125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 7
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
125000003545 alkoxy group Chemical group 0.000 claims description 6
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 5
229910052799 carbon Inorganic materials 0.000 claims description 4
125000003302 alkenyloxy group Chemical group 0.000 claims description 3
125000000000 cycloalkoxy group Chemical group 0.000 claims description 3
125000002071 phenylalkoxy group Chemical group 0.000 claims description 3
IIVWHGMLFGNMOW-UHFFFAOYSA-N 2-methylpropane Chemical compound C[C](C)C IIVWHGMLFGNMOW-UHFFFAOYSA-N 0.000 claims description 2
125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 claims description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 claims 4
125000000217 alkyl group Chemical group 0.000 claims 2
125000004432 carbon atom Chemical group C* 0.000 claims 2
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 1
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract description 3
125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract description 2
125000001424 substituent group Chemical group 0.000 abstract 1
-1 C3-C1S alkenoyloxy Chemical group 0.000 description 88
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CKPKHTKLLYPGFM-UHFFFAOYSA-N 6,6-dimethylheptane-1,1-diol Chemical compound CC(CCCCC(O)O)(C)C CKPKHTKLLYPGFM-UHFFFAOYSA-N 0.000 description 4
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