所有图片(1)
别名:
N-(叔丁氧羰基)-L-苯基丙氨酸, Boc-L-苯丙氨酸
线性分子式:
C6H5CH2CH(COOH)NHCOOC(CH3)3
CAS号:
分子量:
265.30
Beilstein:
2219729
EC 号:
MDL编号:
UNSPSC代码:
12352209
eCl@ss:
32160406
PubChem化学物质编号:
NACRES:
NA.22
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质量水平
检测方案
≥99.0% (T)
形式
solid
旋光性
[α]20/D +25±1°, c = 1% in ethanol
反应适用性
reaction type: Boc solid-phase peptide synthesis
reaction type: C-H Activation
reagent type: ligand
reaction type: Peptide Synthesis
mp
85-87 °C (lit.)
应用
peptide synthesis
官能团
amine
carboxylic acid
SMILES字符串
CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(O)=O
InChI
1S/C14H19NO4/c1-14(2,3)19-13(18)15-11(12(16)17)9-10-7-5-4-6-8-10/h4-8,11H,9H2,1-3H3,(H,15,18)(H,16,17)/t11-/m0/s1
InChI key
ZYJPUMXJBDHSIF-NSHDSACASA-N
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相关类别
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Yong Chen et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 99, 103-113 (2015-12-22)
The objective was to investigate the topical iontophoretic delivery of a series of amino acid ester prodrugs of aciclovir (ACV-X, where ACV=aciclovir and X=Arg, Gly, Ile, Phe, Trp and Val) as a means to enhance cutaneous delivery of ACV. The
Matthew J Crawford et al.
Journal of nucleic acids, 2011, 652702-652702 (2011-07-22)
Conformationally preorganized peptide nucleic acids (PNAs) have been synthesized through backbone modifications at the γ-position, where R = alanine, valine, isoleucine, and phenylalanine side chains. The effects of these side-chains on the conformations and hybridization properties of PNAs were determined
Jie Chen et al.
Archives of pharmacal research, 37(1), 142-148 (2013-11-23)
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