860700
Z-Ser-OH
≥99%
别名:
Z-L-丝氨酸, 苄氧羰基-L-丝氨酸
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关于此项目
线性分子式:
HOCH2CH(NHCO2CH2C6H5)CO2H
化学文摘社编号:
分子量:
239.22
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
EC Number:
214-546-4
Beilstein/REAXYS Number:
2058314
MDL number:
Quality Level
assay
≥99%
form
crystals
optical activity
[α]20/D +5.8°, c = 2.7 in acetic acid
reaction suitability
reaction type: solution phase peptide synthesis
mp
116-119 °C (lit.)
application(s)
peptide synthesis
SMILES string
OC[C@H](NC(=O)OCc1ccccc1)C(O)=O
InChI
1S/C11H13NO5/c13-6-9(10(14)15)12-11(16)17-7-8-4-2-1-3-5-8/h1-5,9,13H,6-7H2,(H,12,16)(H,14,15)/t9-/m0/s1
InChI key
GNIDSOFZAKMQAO-VIFPVBQESA-N
Application
肽合成的结构单元；通过 β-内酯合成各种 α-氨基酸的原料
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
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Jay M West et al.
PloS one, 7(8), e43877-e43877 (2012-09-07)
The mechanism of inactivation of human enzyme N-acylethanolamine-hydrolyzing acid amidase (hNAAA), with selected inhibitors identified in a novel fluorescent based assay developed for characterization of both reversible and irreversible inhibitors, was investigated kinetically and using matrix-assisted laser desorption/ionization time-of-flight mass
M Sypniewski et al.
The Journal of organic chemistry, 65(20), 6595-6600 (2000-10-29)
The enantiospecific synthesis of (R)-Boc-(Fmoc)-aminoglycine 7 was achieved. (S)-Cbz-serine 1 was reacted with diphenylphosphoryl azide in the presence of triethylamine to yield cyclic (S) carbamate 2. The ring nitrogen of 2 was protected with a Boc group (3). The cyclic
Jason Lejeune et al.
Biosensors & bioelectronics, 25(3), 604-608 (2009-03-27)
Changes detected in the imprinting effect by OMNiMIPs imprinted with multiple templates appear to be a function of the maximum template loading. Below the maximum template loading, the polymers imprinted with multiple compounds provide molecular recognition close to the polymers
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 860700-25G | 04061832643090 |