46920
9-芴甲基 N-琥珀酰亚胺基碳酸酯
≥98.0% (HPLC), for peptide synthesis
别名:
9-芴甲基 N-琥珀酰亚氨基碳酸酯, N-(9-芴甲氧羰基氧基)琥珀酰亚胺, Fmoc-OSu
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关于此项目
经验公式（希尔记法）:
C19H15NO5
CAS Number:
分子量:
337.33
Beilstein:
3569540
EC 号:
MDL编号:
UNSPSC代码:
12352108
PubChem化学物质编号:
NACRES:
NA.22
Product Name
9-芴甲基 N-琥珀酰亚胺基碳酸酯, ≥98.0% (HPLC)
质量水平
方案
≥98.0% (HPLC)
表单
powder
mp
150-153 °C (lit.)
应用
peptide synthesis
官能团
Fmoc
imide
储存温度
2-8°C
SMILES字符串
O=C(OCC1c2ccccc2-c3ccccc13)ON4C(=O)CCC4=O
InChI
1S/C19H15NO5/c21-17-9-10-18(22)20(17)25-19(23)24-11-16-14-7-3-1-5-12(14)13-6-2-4-8-15(13)16/h1-8,16H,9-11H2
InChI key
WMSUFWLPZLCIHP-UHFFFAOYSA-N
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应用
选择性制备羟基-氨基酸 N-(9-芴甲氧羰基)衍生物的最有效试剂，反应具有高产率。比与氯甲酸酯、Fmoc-Cl 作用时的二肽形成率低。已用于合成糖肽。
警示用语：
Warning
危险分类
Acute Tox. 4 Oral - Aquatic Chronic 2 - Skin Sens. 1
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
Eyeshields, Gloves, type N95 (US)
Improved purities for Fmoc-amino acids from Fmoc-ONSu.
R C Milton et al.
International journal of peptide and protein research, 30(3), 431-432 (1987-09-01)
Occupational airborne allergic contact dermatitis from succinimidyl carbonates.
J F Fowler et al.
Contact dermatitis, 45(1), 38-38 (2001-06-26)
A. Paquet
Canadian Journal of Chemistry, 60, 976-976 (1982)
Huaimin Wang et al.
Scientific reports, 5, 16680-16680 (2015-11-18)
Biocompatible peptide-based supramolecular hydrogel has recently emerged as a new and promising system for biomedical applications. In this work, Rhodamine B is employed as a new capping group of self-assembling peptide, which not only provides the driving force for supramolecular
Ning Wang et al.
Carbohydrate research, 411, 37-41 (2015-05-15)
Monoglucosylated high-mannose-type glycan (Glc1Man9GlcNAc2: G1M9) is well-known as a key glycoform in the glycoprotein folding process, which is specifically recognized by lectin chaperones calnexin (CNX) and calreticulin (CRT) in the endoplasmic reticulum (ER). In this work, we developed an efficient
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