JPS6245235B2 - - Google Patents
Info
- Publication number
- JPS6245235B2 JPS6245235B2 JP272784A JP272784A JPS6245235B2 JP S6245235 B2 JPS6245235 B2 JP S6245235B2 JP 272784 A JP272784 A JP 272784A JP 272784 A JP272784 A JP 272784A JP S6245235 B2 JPS6245235 B2 JP S6245235B2
- Authority
- JP
- Japan
- Prior art keywords
- chloroethylureido
- propyltriethoxysilane
- polysilsesquioxane
- days
- values
- 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.)
- Expired
Links
- LUCAQMQXQLTHEQ-UHFFFAOYSA-N 1-(2-chloroethyl)-3-(3-triethoxysilylpropyl)urea Chemical compound CCO[Si](OCC)(OCC)CCCNC(=O)NCCCl LUCAQMQXQLTHEQ-UHFFFAOYSA-N 0.000 claims description 9
- 229920000734 polysilsesquioxane polymer Polymers 0.000 description 8
- 238000010521 absorption reaction Methods 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- -1 ureido carbonyl groups Chemical group 0.000 description 6
- 239000007787 solid Substances 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000012488 sample solution Substances 0.000 description 4
- 230000004083 survival effect Effects 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 3
- 238000000862 absorption spectrum Methods 0.000 description 3
- 150000001721 carbon Chemical group 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 238000000921 elemental analysis Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 3
- 230000001766 physiological effect Effects 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- BCMYXYHEMGPZJN-UHFFFAOYSA-N 1-chloro-2-isocyanatoethane Chemical compound ClCCN=C=O BCMYXYHEMGPZJN-UHFFFAOYSA-N 0.000 description 2
- 241000699670 Mus sp. Species 0.000 description 2
- 230000001093 anti-cancer Effects 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000002504 physiological saline solution Substances 0.000 description 2
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 2
- 229920000053 polysorbate 80 Polymers 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 2
- VKPPFDPXZWFDFA-UHFFFAOYSA-N 2-chloroethanamine Chemical compound NCCCl VKPPFDPXZWFDFA-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 210000000683 abdominal cavity Anatomy 0.000 description 1
- 230000007059 acute toxicity Effects 0.000 description 1
- 231100000403 acute toxicity Toxicity 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 238000003760 magnetic stirring Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000004682 monohydrates Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- FRGPKMWIYVTFIQ-UHFFFAOYSA-N triethoxy(3-isocyanatopropyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCN=C=O FRGPKMWIYVTFIQ-UHFFFAOYSA-N 0.000 description 1
- 239000011345 viscous material Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP272784A JPS59144792A (ja) | 1984-01-12 | 1984-01-12 | 3−(β−クロロエチルウレイド)プロピルトリエトキシシラン |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP272784A JPS59144792A (ja) | 1984-01-12 | 1984-01-12 | 3−(β−クロロエチルウレイド)プロピルトリエトキシシラン |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18140880A Division JPS57105423A (en) | 1980-12-23 | 1980-12-23 | Chloroethylureidopropylpolysilsesquioxane |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59144792A JPS59144792A (ja) | 1984-08-18 |
JPS6245235B2 true JPS6245235B2 (es) | 1987-09-25 |
Family
ID=11537342
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP272784A Granted JPS59144792A (ja) | 1984-01-12 | 1984-01-12 | 3−(β−クロロエチルウレイド)プロピルトリエトキシシラン |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59144792A (es) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102014209239A1 (de) | 2014-05-15 | 2015-11-19 | Evonik Degussa Gmbh | Harnstoffhaltige Silane, Verfahren zu deren Herstellung und deren Verwendung |
DE102014209226A1 (de) | 2014-05-15 | 2015-11-19 | Evonik Degussa Gmbh | Harnstoffhaltige Silane, Verfahren zu deren Herstellung und deren Verwendung |
DE102014209233A1 (de) * | 2014-05-15 | 2015-11-19 | Evonik Degussa Gmbh | Harnstoffhaltige Mercaptosilane, Verfahren zu deren Herstellung und deren Verwendung |
DE102014209221A1 (de) * | 2014-05-15 | 2015-11-19 | Evonik Degussa Gmbh | Verfahren zur Herstellung von harnstoffhaltigen Mercaptosilanen |
-
1984
- 1984-01-12 JP JP272784A patent/JPS59144792A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS59144792A (ja) | 1984-08-18 |
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