| ²é¿´: 131 | »Ø¸´: 3 | ||
| µ±Ç°Ö÷ÌâÒѾ´æµµ¡£ | ||
| ¡¾ÐüÉͽð±Ò¡¿»Ø´ð±¾ÌûÎÊÌ⣬×÷Õ߯ó¶ì½«ÔùËÍÄú 7 ¸ö½ð±Ò | ||
[ÇóÖú]
4-äå-2,3,5,6-ËÄ·ú±½ÒÒËáµÄÓÃ;[ÓÐЧÆÚÖÁ2008Äê07ÔÂ20ÈÕ]
|
||
|
4-äå-2,3,5,6-ËÄ·ú±½ÒÒËáÓ¦ÓûòÓÃ;µÄÏà¹ØÎÄÏ×,ÖÐÓ¢ÎÄ½Ô¿É [ Last edited by zzgyb on 2008-8-18 at 11:35 ] |
» ²ÂÄãϲ»¶
Ò»Ö¾Ô¸°²´óÉúÎïѧ07³õÊÔ322¡¢±¾¿Æ¶þ±¾¡¢µ÷¼ÁÇóÖú
ÒѾÓÐ7È˻ظ´
0856ר˶Çóµ÷¼Á Ï£ÍûÊÇaÇøÔºÐ£
ÒѾÓÐ25È˻ظ´
085600²ÄÁÏÓ뻯¹¤£¬Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Ò»Ö¾Ô¸2110£¬»¯Ñ§Ñ§Ë¶310·Ö£¬±¾¿ÆÖصãË«·ÇÇóµ÷¼Á
ÒѾÓÐ19È˻ظ´
²ÄÁϹ¤³Ì085601£¬270Çóµ÷¼Á
ÒѾÓÐ33È˻ظ´
¸´ÊÔµ÷¼Á
ÒѾÓÐ12È˻ظ´
ÐÂÒ»´úµç×ÓÐÅÏ¢294Çóµ÷¼Á ²»ÌôѧУ
ÒѾÓÐ8È˻ظ´
290µ÷¼ÁÉúÎï0860
ÒѾÓÐ29È˻ظ´
279ѧ˶ʳƷרҵÇóµ÷¼ÁԺУ
ÒѾÓÐ15È˻ظ´
310Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
zsma
ľ³æ (ÖøÃûдÊÖ)
Сľ³æÖ®¶þµ±¼Ò
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ¹ó±ö: 1.308
- ½ð±Ò: 1555.9
- É¢½ð: 311
- ºì»¨: 1
- Ìû×Ó: 1143
- ÔÚÏß: 81.7Сʱ
- ³æºÅ: 298894
- ×¢²á: 2006-11-19
- ÐÔ±ð: GG
- רҵ: ¹ÌÌåÁ¦Ñ§

2Â¥2008-07-17 10:59:33
renlintyut
Òø³æ (СÓÐÃûÆø)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 216
- Ìû×Ó: 57
- ÔÚÏß: 10.2Сʱ
- ³æºÅ: 482438
- ×¢²á: 2007-12-23
3Â¥2008-07-18 12:42:40
neuron2004
½ð³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 483.3
- É¢½ð: 456
- ºì»¨: 2
- Ìû×Ó: 1137
- ÔÚÏß: 91.7Сʱ
- ³æºÅ: 225328
- ×¢²á: 2006-03-22
- ÐÔ±ð: GG
- רҵ: Éñ¾ÉúÎïѧ
¡ï ¡ï ¡ï
Æó¶ì(½ð±Ò+3,VIP+0):лл°ïæ
Æó¶ì(½ð±Ò+3,VIP+0):лл°ïæ
|
The [4-amino(mono- or poly-fluoro)phenyl]alkanoic acids and esters required as intermediates are prepared by a sequence of reactions involving nitration of a suitable phenylalkanoic acid followed by reduction of the nitro group. For example, 2,3,5,6-tetrafluorophenylacetic acid is converted to 4-amino-2,3,5,6-tetrafluorophenylacetic acid by this method. The [4-amino-(mono- or poly-fluoro)benzoyl]alkanoic acids and esters are prepared by the reaction of ammonia or sodium amide with (4-halobenzoyl)alkanoic acids. For example, the reaction of sodium amide with ethyl 2,3,4,5,6-pentafluorobenzoylacetate yields ethyl(4-amino-2,3,5,6-tetrafluorobenzoyl)acetate. http://www.freepatentsonline.com/4243609.html |
4Â¥2008-07-18 22:06:04













»Ø¸´´ËÂ¥