FMOC-MET(O2)-OH
FMOC-MET(O2)-OH 物理性質
- 沸点 :
- 709.5±60.0 °C(Predicted)
- 比重(密度) :
- 1.359
- 貯蔵温度 :
- Sealed in dry,Room Temperature
- 溶解性:
- Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
- 酸解離定数(Pka):
- 3.52±0.10(Predicted)
- 外見 :
- 粉
- 色:
- 白い
- 主な用途:
- peptide synthesis
- InChI:
- InChI=1S/C20H21NO6S/c1-28(25,26)11-10-18(19(22)23)21-20(24)27-12-17-15-8-4-2-6-13(15)14-7-3-5-9-16(14)17/h2-9,17-18H,10-12H2,1H3,(H,21,24)(H,22,23)/t18-/m0/s1
- InChIKey:
- KJLKPACOHZKRFM-SFHVURJKSA-N
- SMILES:
- C(O)(=O)[C@@H](NC(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O)CCS(C)(=O)=O
- CAS データベース:
- 163437-14-7(CAS DataBase Reference)
FMOC-MET(O2)-OH 価格
もっと(12)
| メーカー |
製品番号 |
製品説明 |
CAS番号 |
包装 |
価格 |
更新時間 |
購入 |
|
富士フイルム和光純薬株式会社(wako)
|
W01MAS099866 |
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)-amino)-4-(methylsulfonyl)butanoic acid |
163437-14-7 |
1g |
￥31300 |
2024-03-01 |
購入 |
|
富士フイルム和光純薬株式会社(wako)
|
W01COBSS-8750 |
Fmoc-Met(O2)-OH |
163437-14-7 |
1g |
￥12500 |
2024-03-01 |
購入 |
|
富士フイルム和光純薬株式会社(wako)
|
W01FLCM06257 |
Fmoc-Met(O2)-OH |
163437-14-7 |
25g |
￥83100 |
2024-03-01 |
購入 |
|
富士フイルム和光純薬株式会社(wako)
|
W01COBSS-8750 |
Fmoc-Met(O2)-OH |
163437-14-7 |
5g |
￥42500 |
2024-03-01 |
購入 |
|
関東化学株式会社(KANTO)
|
49928-64 |
Ｆｍｏｃ‐Ｍｅｔ（Ｏ２）‐ＯＨ
Fmoc‐Met(O2)‐OH |
163437-14-7 |
5g |
￥9520 |
2024-07-01 |
購入 |
FMOC-MET(O2)-OH 化学特性,用途語,生産方法
説明
FMOC-Met (O2)-OH is the N-alpha protected form of L-methionine mediated by FMOC group (9-Fluorenylmethyloxycarbonyl). It is useful to act as a building block in peptide synthesis. For example, it, as well as its derivative Tbfmoc-Met-OH can be used as a building block for the solid phase synthesis of ubiquitin C-hydrazide. It can also be used for synthesizing some novel cyclic peptides with pharmacological effects such as treatment of inflammatory disease.
化学的特性
White powder
参考文献
http://www.sigmaaldrich.com/technical-documents/articles/chemfiles/natural-amino-acid.html
https://www.iris-biotech.de/de/faa1490/Anderson, S. N., et al. "Microarrayed compound screening (microARCS) to identify activators and inhibitors of AMP-activated protein kinase."Journal of Biomolecular Screening 9.2(2004):112-121.
http://web.b.ebscohost.com/abstractdirect=true&profile=ehost&scope=site&authtype=crawler&jrnl=09707077&AN=103358230&=iEFjDXbrcrGANWWK7vpLdmsN8yhCmNraNdm1aLMwCgXjuCpr9xSGhioVTsYZqXmo5JtrShPp2WNBkVHpx75ovQ%3d%3d&crl=c&resultNs=AdminWebAuth&resultLocal=ErrCrlNotAuth&crlhashurl=login.aspx%3fdirect%3dtrue%26profile%3dehost%26scope%3dsite%26authtype%3dcrawler%26jrnl%3d09707077%26AN%3d103358230
http://www.google.com/patents/US6511961
FMOC-MET(O2)-OH 上流と下流の製品情報
原材料
準備製品
FMOC-MET(O2)-OH 生産企業
Global( 120)Suppliers
FMOC-MET(O2)-OH スペクトルデータ(1HNMR)
163437-14-7(FMOC-MET(O2)-OH)キーワード:
- 163437-14-7
- FMOC-L-METHIONINE-SULFONE
- FMOC-L-MET(O2)-OH
- FMOC-METHIONINE(O2)-OH
- FMOC-MET(O2)-OH
- (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-4-(methylsulfonyl)butanoic acid
- FMoc-Met(O)2-OH FMoc-L-Methionine sulfone
- N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-L-METHIONINE SULFONE
- N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-L-METHIONINESULFON
- N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-L-METHIONINESULFONE
- N-ALPHA-FMOC-L-METHIONINE-SULFONE
- (2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-methanesulfonylbutanoic acid
- N-FMoc-L-Methionine sulfone, 98%
- Fmoc-L-methionine sulfone≥ 98% (HPLC)
- (9H-Fluoren-9-yl)MethOxy]Carbonyl Met(O2)-OH
- Butanoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-4-(methylsulfonyl)-, (2S)-
- (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-methylsulfonylbutanoic acid
- (S)-2-(Fmoc-amino)-4-(methylsulfonyl)butanoic Acid
- Fmoc-Met(O2)
- FMOC-MET(O2)-OH
- FMOC‐MET(O2)‐OH