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Merck
CN

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
化学文摘社编号:
分子量:
337.33
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352108
EC Number:
433-520-5
MDL number:
Beilstein/REAXYS Number:
3569540
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产品名称

9-芴甲基 N-琥珀酰亚胺基碳酸酯, ≥98.0% (HPLC)

InChI key

WMSUFWLPZLCIHP-UHFFFAOYSA-N

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

SMILES string

O=C(OCC1c2ccccc2-c3ccccc13)ON4C(=O)CCC4=O

assay

≥98.0% (HPLC)

form

powder

mp

150-153 °C (lit.)

application(s)

peptide synthesis

functional group

Fmoc
imide

storage temp.

2-8°C

Quality Level

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Application

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。

pictograms

Exclamation markEnvironment

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Skin Sens. 1

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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分析证书(COA)

Lot/Batch Number

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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
Occupational airborne allergic contact dermatitis from succinimidyl carbonates.
J F Fowler et al.
Contact dermatitis, 45(1), 38-38 (2001-06-26)
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)
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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