±±¾©Ê¯ÓÍ»¯¹¤Ñ§Ôº2026ÄêÑо¿ÉúÕÐÉú½ÓÊÕµ÷¼Á¹«¸æ
²é¿´: 321  |  »Ø¸´: 1

wei339567149

½ð³æ (СÓÐÃûÆø)

[ÇóÖú] ÇóÖú΢Æ×Êý¾Ý ÒÑÓÐ1È˲ÎÓë

̼Æ×Êý¾Ý£º£¨LA-42£©

29.9,36.0,50.8,55.4,114.0,114.0,129.3,129.3,132.4,158.2,178.8
»Ø¸´´ËÂ¥

» ²ÂÄãϲ»¶

» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:

LV
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

wangkaibo123

ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)

kerry

ÓÅÐã°æÖ÷

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
wei339567149: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-12-24 14:56:58
²éѯģʽ£ºÄ£ºý²éѯ
̼Æ×Êý¾ÝÊäÈ룺
°´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺
21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2

ÈܼÁÑ¡Ï
Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨)
ÏàËÆ¶È£º   %(ÏàËÆ¶È>=50%)



²éѯ½á¹û£º¹²²éµ½269¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     (¡À)-trans-2,4-bis(4-methoxyphenethyl)azetidine
C21H27NO2     ÏàËÆ¶È:81.8%
Bioorganic & Medicinal Chemistry          2013          21          6771-6777
Synthesis and evaluation of novel azetidine analogs as potent inhibitors of vesicular [3H]dopamine uptake
Derong Ding, Justin R. Nickell, Agripina G. Deaciuc, Narsimha Reddy Penthala, Linda P. Dwoskin, Peter A. Crooks
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     p-methoxyphenylpropionic acid
    ÏàËÆ¶È:72.7%
Chinese Traditional and Herbal Drugs          2009          40          512-516
ǧ½ï°Î»¯Ñ§³É·ÖÑо¿
À;ÑîÃÀ»ª;˹½¨ÓÂ;ÂíС¾ü;çѽ£»ª
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     Dihydo p-methoxy cinnamic acid
    ÏàËÆ¶È:72.7%
Pharmazie          2010          65          913-918
Tyrosinase inhibitory activities of cinnamic acid analogues
T.Takahashi and M.Miyazawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     cis-2,4-bis(4-methoxyphenethyl)azetidine
C21H27NO2     ÏàËÆ¶È:69.2%
Bioorganic & Medicinal Chemistry          2013          21          6771-6777
Synthesis and evaluation of novel azetidine analogs as potent inhibitors of vesicular [3H]dopamine uptake
Derong Ding, Justin R. Nickell, Agripina G. Deaciuc, Narsimha Reddy Penthala, Linda P. Dwoskin, Peter A. Crooks
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     2-benzazepines
C12H15NO2     ÏàËÆ¶È:66.6%
Bioorganic & Medicinal Chemistry Letters          2009          19          3193-3195
An efficient preparation of N-alkyl-2-benzazepine derivatives and investigation of their biological activity
Akio Kamimura, Masahiro So, Tomohiro Kuratani, Kenji Matsuura, Makoto Inui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     N-methoxy-3-(4-methylphenyl)propionamide
C11H15NO2     ÏàËÆ¶È:63.6%
Heterocycles          2003          59          149-160
Synthesis of Spiro-fused Nitrogen Heterocyclic Compounds via N-Methoxy-N-acylnitrenium Ions Using Phenyliodine(III) Bis(trifluoroacetate) in Trifluoroethanol
Etsuko Miyazawa, Takeshi Sakamoto, and Yasuo Kikugawa*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (2R,3R)-and (2S,3S)-2,3-Bis-(4-methoxybenzyl)-1,-4-diphenylbutane-1,4-dione
C32H30O4     ÏàËÆ¶È:63.6%
Journal of the Chemical Society, Perkin Transactions 1          1989                   1585-1591
Medicinal plants of Southern Africa. Part 4. Synthesis of brackenin-like molecules from 1,4-dicarbonyl precursors and by oxidative coupling. X-Ray molecular structure of racemic-2,3-dibenzyl-1,4-diphenylbutane-1,4-dione
Siegfried E. Drewes, Craig J. Hogan, Perry T. Kaye and Gregory H. P. Roos
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     3-(4-Methoxybenzyl)thiophene
    ÏàËÆ¶È:63.6%
Tetrahedron          2012          68          3956-3962
Palladium-catalyzed coupling reactions of (ArCH2)Ti(O-i-Pr)3 with aromatic or heteroaromatic bromides
Shu-Ting Chang, Qinghan Li, Ruei-Tang Chiang, Han-Mou Gau
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     4-cyano-N-(4-methoxybenzyl)benzenesulfonamide
C15H14N2O3S     ÏàËÆ¶È:63.6%
Journal of Heterocyclic Chemistry          2011          48          407-413
Biaryl sulfonamides from O-acetyl amidoximes: 1,2,4-Oxadiazole cyclization under acidic conditions
Stefan Dosa, Jörg Daniels and Michael G¨¹tschow
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     compound
C12H24O2Si     ÏàËÆ¶È:63.6%
European Journal of Organic Chemistry          2011                   6039-6055
Towards the Synthesis of the 4,19-Diol Derivative of (¨C)-Mycothiazole: Synthesis of a Potential Key Intermediate
Fr¨¦d¨¦ric Batt and Fabienne Fache
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     (4-methoxy-benzyl)-p-tolyl-amine
C15H17NO     ÏàËÆ¶È:63.6%
Tetrahedron          2013          69          7988-7994
In(OTf)3 catalyzed N-benzylation of amines utilizing benzyl alcohols in water
Jin-Ming Yang, Ran Jiang, Lin Wu, Xiao-Ping Xu, Shun-Yi Wang, Shun-Jun Ji
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     7-(4-methoxyphenyl)-6,7-dihydrothieno[2,3-b]pyrazine
C13H12N2OS     ÏàËÆ¶È:63.6%
Heterocycles          2013          87          1507-1517
A Convenient Two-Step Synthesis of 7-Aryl-6,7-dihydrothieno[2,3-b]pyrazines from Aryl(3-chloropyrazin-2-yl)methanones
Kazuhiro Kobayashi,* Teruhiko Suzuki, and Naoki Matsumoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     4-methoxy-phenethylamine
    ÏàËÆ¶È:63.6%
Organic Magnetic Resonance          1983          21          391-396
13C NMR spectra and structure of mono-, di- and trimethoxyphenylethylamines and amphetamines
Keith Bailey and Donald Legault
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     2-(4-methoxyphenyl)ethanamine
    ÏàËÆ¶È:63.6%
Organic Magnetic Resonance          1983          21          443-449
Empirical additive parameter and automatic assignment of 13C NMR signals of some aryl and heteroaryl groups. A new criterion for a linear relationship between 13C chemical shifts and charge densities
Ivan P. Bangov and Reiner Radeglia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     N-(4-Methoxybenzyl)benzenamine
C14H15NO     ÏàËÆ¶È:63.6%
Tetrahedron          2013          69          9145-9154
Efficient and chemoselective direct reductive amination of aromatic aldehydes catalyzed by oxo¨Crhenium complexes containing heterocyclic ligands
Joana R. Bernardo, Sara C.A. Sousa, Pedro R. Florindo, Mariusz Wolff, Barbara Machura, Ana C. Fernandes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
2Â¥2013-12-24 11:34:44
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ wei339567149 µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] Ò»Ö¾Ô¸Ö£ÖÝ´óѧ²ÄÁÏÓ뻯¹¤085600£¬Çóµ÷¼Á +19 ³ÔµÄ²»ÉÙ 2026-04-02 19/950 2026-04-04 10:26 by À´¿´Á÷ÐÇÓê10
[¿¼ÑÐ] ²ÄÁÏ295 +13 СӢ11 2026-04-03 14/700 2026-04-04 09:02 by À´¿´Á÷ÐÇÓê10
[¿¼ÑÐ] 283Çóµ÷¼Á +5 A child 2026-03-28 5/250 2026-04-04 00:40 by userper
[¿¼ÑÐ] ×Ü·Ö328ÉúÎïÓëÒ½Ò©¿¼ÊýѧÇóµ÷¼Á +7 aaadim 2026-04-02 9/450 2026-04-03 22:53 by syh9288
[¿¼ÑÐ] ¿¼ÑÐÇóµ÷¼Á +3 ľÐÄÏë¼ÌÐøÉîÔì 2026-04-03 3/150 2026-04-03 21:56 by à£à£à£0119
[¿¼ÑÐ] ר˶085601Çóµ÷¼Á +7 suyifei 2026-04-03 8/400 2026-04-03 14:00 by ÐÀϲ777
[¿¼ÑÐ] Çó²ÄÁϵ÷¼Á Ò»Ö¾Ô¸Äϲý´óѧ 328·Ö +5 yyy..... 2026-04-03 5/250 2026-04-03 13:46 by °ÙÁéͯ888
[¿¼ÑÐ] 319Çóµ÷¼Á +18 Ì«ÈÝÒ×1018 2026-04-01 18/900 2026-04-03 11:18 by linyelide
[¿¼ÑÐ] Ò»Ö¾Ô¸°²»Õ´óѧ0817»¯Ñ§¹¤³ÌÓë¼¼Êõ£¬Çóµ÷¼Á +14 ÎÒ²»ÊÇÖ»Òò 2026-04-02 15/750 2026-04-03 09:49 by À¶ÔÆË¼Óê
[¿¼ÑÐ] 309Çóµ÷¼Á +14 ´ô¹½²»ÊÇ´÷·ò 2026-04-02 14/700 2026-04-03 09:42 by À¶ÔÆË¼Óê
[¿¼ÑÐ] ÖØÇì´óѧ²ÄÁÏÓ뻯¹¤085600£¬³õÊÔ370+£¬ÇóÇóµ÷¼Á½¨Òé +8 shzhou_ 2026-04-01 9/450 2026-04-03 09:31 by À¶ÔÆË¼Óê
[¿¼²©] É격ÇóÖú +3 Reee1Llll 2026-04-01 3/150 2026-04-02 22:29 by ÕâÊÇÒ»¸öÎÞÁĵÄê
[¿¼ÑÐ] »¯Ñ§070300-×Ü·Ö378-Çóµ÷¼Á +5 ŲÒÎ×ÓµÄÅÝÅÝÌÇ 2026-04-02 5/250 2026-04-02 22:20 by ZXlzxl0425
[¿¼ÑÐ] »·¾³¿ÆÑ§Ó빤³Ì334·ÖÇóµ÷¼Á +7 ÍõÒ»Ò»ÒÀÒÀ 2026-03-30 9/450 2026-04-02 21:15 by 1104338198
[¿¼ÑÐ] 293Çóµ÷¼Á +4 çæçæÀÖ 2026-04-02 4/200 2026-04-02 20:10 by 6781022
[¿¼ÑÐ] Ò»Ö¾Ô¸ÉϺ£º£Ñó´óѧ083200ʳƷѧ˶£¬Çóµ÷¼Á£¬½ÓÊÜÆäËûרҵ +6 whatÕÅ 2026-04-01 7/350 2026-04-02 16:48 by zzsw+
[¿¼ÑÐ] 282Çóµ÷¼Á +13 ºôÎü¶¼ÊǼõ·Ê 2026-04-01 13/650 2026-04-02 14:10 by baoball
[¿¼ÑÐ] 352·Ö-085602-Ò»Ö¾Ô¸985 +6 º£Äɰٴ¨Ly 2026-03-29 6/300 2026-03-31 21:06 by yuq
[¿¼ÑÐ] 080200ѧ˶£¬»úе¹¤³Ìרҵ277·Ö£¬Çó´ø×ߣ¡ +4 Æ¿×ÓPZ 2026-03-31 4/200 2026-03-31 20:16 by vgtyfty
[¿¼ÑÐ] 11408Èí¼þ¹¤³ÌÇóµ÷¼Á +3 Qiuѧing 2026-03-28 3/150 2026-03-28 21:50 by zhq0425
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û