所有图片(2)
About This Item
经验公式(希尔记法):
C15H13NO3
CAS号:
分子量:
255.27
Beilstein:
7712144
MDL编号:
UNSPSC代码:
12352005
PubChem化学物质编号:
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方案
≥99.0%
mp
164.5 °C (lit.)
应用
peptide synthesis
SMILES字符串
ONC(=O)OCC1c2ccccc2-c3ccccc13
InChI
1S/C15H13NO3/c17-15(16-18)19-9-14-12-7-3-1-5-10(12)11-6-2-4-8-13(11)14/h1-8,14,18H,9H2,(H,16,17)
InChI key
HHNJBGORPSTJDX-UHFFFAOYSA-N
应用
9-Fluorenylmethyl N-hydroxycarbamate (Fmoc-NHOH) can be used as a reactant to prepare:
- N-Fmoc-aminooxy-2-chlorotrityl polystyrene, a solid-phase resin used to produce hydroxamic acids and peptidyl hydroxamic acids.
- 9-Fluorenylmethyl nosyloxycarbamate (Fmoc-NHONs) by reacting with nosyl chloride.
其他说明
在氯三苯甲基树脂上固相合成(肽)异羟肟酸类化合物时用到的结构单元
警示用语:
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
N-Fmoc-aminooxy-2-chlorotrityl polystyrene resin: A facile solid-phase methodology for the synthesis of hydroxamic acids
Mellor SL, et al.
Tetrahedron Letters, 38(18), 3311-3314 (1997)
Synthesis of N-protected cyano aziridines
Fioravanti S, et al.
Synlett, 2004(06), 1083-1085 (2004)
S.L. Mellor et al.
Tetrahedron Letters, 38, 3311-3311 (1997)
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