215333
D-对羟基苯甘氨酸
≥98%
别名:
(R)-2-氨基-2-(4-羟基苯)乙酸
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关于此项目
线性分子式:
HOC6H4CH(NH2)CO2H
化学文摘社编号:
分子量:
167.16
Beilstein:
2210998
EC 号:
MDL编号:
UNSPSC代码:
41116107
eCl@ss:
32160406
PubChem化学物质编号:
NACRES:
NA.22
方案
≥98%
表单
solid
旋光性
[α]23/D −158±3°, c = 1 in 1 M HCl
反应适用性
reaction type: solution phase peptide synthesis
mp
240 °C (dec.) (lit.)
应用
peptide synthesis
SMILES字符串
N[C@@H](C(O)=O)c1ccc(O)cc1
InChI
1S/C8H9NO3/c9-7(8(11)12)5-1-3-6(10)4-2-5/h1-4,7,10H,9H2,(H,11,12)/t7-/m1/s1
InChI key
LJCWONGJFPCTTL-SSDOTTSWSA-N
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储存分类代码
13 - Non 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
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Tony Ly et al.
Journal of the American Society for Mass Spectrometry, 20(6), 1148-1158 (2009-03-17)
Photodissociation of iodo-tyrosine modified peptides yields localized radicals on the tyrosine side chain, which can be further dissociated by collisional activation. We have performed extensive experiments on model peptides, RGYALG, RGYG, and their derivatives, to elucidate the mechanisms underlying backbone
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