JP2000327617A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2000327617A5 JP2000327617A5 JP1999327155A JP32715599A JP2000327617A5 JP 2000327617 A5 JP2000327617 A5 JP 2000327617A5 JP 1999327155 A JP1999327155 A JP 1999327155A JP 32715599 A JP32715599 A JP 32715599A JP 2000327617 A5 JP2000327617 A5 JP 2000327617A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- oxystyrene
- represented
- embedded image
- derivative
- 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.)
- Granted
Links
- 238000000034 method Methods 0.000 description 6
- 238000004821 distillation Methods 0.000 description 5
- 0 C*(C)OCc1cccc(C=C)c1 Chemical compound C*(C)OCc1cccc(C=C)c1 0.000 description 4
- 150000002828 nitro derivatives Chemical class 0.000 description 3
- 150000002832 nitroso derivatives Chemical class 0.000 description 3
- UFBJCMHMOXMLKC-UHFFFAOYSA-N 2,4-dinitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O UFBJCMHMOXMLKC-UHFFFAOYSA-N 0.000 description 2
- FMFHUEMLVAIBFI-UHFFFAOYSA-N 2-phenylethenyl acetate Chemical group CC(=O)OC=CC1=CC=CC=C1 FMFHUEMLVAIBFI-UHFFFAOYSA-N 0.000 description 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000005103 alkyl silyl group Chemical group 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- DAHPIMYBWVSMKQ-UHFFFAOYSA-N n-hydroxy-n-phenylnitrous amide Chemical compound O=NN(O)C1=CC=CC=C1 DAHPIMYBWVSMKQ-UHFFFAOYSA-N 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- HXLLCROMVONRRO-UHFFFAOYSA-N 2-butoxyethenylbenzene Chemical compound CCCCOC=CC1=CC=CC=C1 HXLLCROMVONRRO-UHFFFAOYSA-N 0.000 description 1
- -1 Oxy styrene derivative Chemical class 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP32715599A JP3879340B2 (ja) | 1998-12-01 | 1999-11-17 | オキシスチレン誘導体の蒸留方法 |
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP34155998 | 1998-12-01 | ||
| JP10-341559 | 1999-03-18 | ||
| JP11-73510 | 1999-03-18 | ||
| JP7351099 | 1999-03-18 | ||
| JP32715599A JP3879340B2 (ja) | 1998-12-01 | 1999-11-17 | オキシスチレン誘導体の蒸留方法 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006165143A Division JP3879775B2 (ja) | 1998-12-01 | 2006-06-14 | オキシスチレン誘導体の蒸留方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2000327617A JP2000327617A (ja) | 2000-11-28 |
| JP2000327617A5 true JP2000327617A5 (enExample) | 2006-07-27 |
| JP3879340B2 JP3879340B2 (ja) | 2007-02-14 |
Family
ID=27301239
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP32715599A Expired - Lifetime JP3879340B2 (ja) | 1998-12-01 | 1999-11-17 | オキシスチレン誘導体の蒸留方法 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3879340B2 (enExample) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1315779C (zh) | 2002-02-15 | 2007-05-16 | 克鲁普顿公司 | 作为阻聚剂的亚硝基苯酚和c－亚硝基苯胺 |
| JP2006335715A (ja) * | 2005-06-03 | 2006-12-14 | Tosoh Corp | 高品質ビニル安息香酸−第３級ブチルエステル及びその製造方法 |
| JP4862323B2 (ja) * | 2005-09-05 | 2012-01-25 | 三菱瓦斯化学株式会社 | 高純度アダマンチル（メタ）アクリレート類の製造方法 |
-
1999
- 1999-11-17 JP JP32715599A patent/JP3879340B2/ja not_active Expired - Lifetime
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2002513793A5 (enExample) | ||
| JP2005525427A5 (enExample) | ||
| JP2006514626A5 (enExample) | ||
| JP2005053931A5 (enExample) | ||
| JP2012506896A5 (enExample) | ||
| JP2006513268A5 (ja) | アンタゴニスト活性を有するベンゾアゾリルピペラジン誘導体 | |
| JP2005508905A5 (enExample) | ||
| JP2007511546A5 (enExample) | ||
| JP2009541363A5 (enExample) | ||
| JP2005511547A5 (enExample) | ||
| JP2002527414A5 (enExample) | ||
| JP2004501940A5 (enExample) | ||
| JP2007246474A5 (enExample) | ||
| JP2002520316A5 (enExample) | ||
| JP2003534359A5 (enExample) | ||
| CA2796933A1 (en) | 1-(2-fluorobiphenyl-4-yl)-alkyl carboxylic acid derivatives for the therapy of transthyretin amyloidosis | |
| JP2007500222A5 (enExample) | ||
| EP1279665A3 (en) | A process for the preparation of perindopril, its analogous compounds and salts thereof using 2,5-dioxo-oxazolidine intermediate compounds | |
| JP2000327617A5 (enExample) | ||
| JP2020504184A5 (enExample) | ||
| JP2005526149A5 (enExample) | ||
| JP2002501094A5 (enExample) | ||
| JP2005520809A5 (enExample) | ||
| JP2004517891A5 (enExample) | ||
| JP2007519685A5 (enExample) |