15380
N-(叔-叔丁氧羰基)-L-丙氨酸
≥99.0% (TLC), for peptide synthesis
别名:
N-(叔丁氧羰基)-L-丙氨酸, Boc-L-丙氨酸
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关于此项目
线性分子式:
CH3CH[NHCO2C(CH3)3]CO2H
化学文摘社编号:
分子量:
189.21
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
239-847-8
MDL number:
Beilstein/REAXYS Number:
1726365
产品名称
N-(叔-叔丁氧羰基)-L-丙氨酸, ≥99.0% (TLC)
Quality Level
assay
≥99.0% (TLC)
optical activity
[α]20/D −25±1°, c = 2% in acetic acid
reaction suitability
reaction type: Boc solid-phase peptide synthesis, reaction type: C-H Activation, reagent type: ligand
reaction type: Peptide Synthesis
mp
79-83 °C (lit.)
application(s)
peptide synthesis
functional group
amine, carboxylic acid
SMILES string
C[C@H](NC(=O)OC(C)(C)C)C(O)=O
InChI
1S/C8H15NO4/c1-5(6(10)11)9-7(12)13-8(2,3)4/h5H,1-4H3,(H,9,12)(H,10,11)/t5-/m0/s1
InChI key
QVHJQCGUWFKTSE-YFKPBYRVSA-N
Application
Boc-Ala-OH可用于：
- 制备N-炔丙基丙氨酸，其是生成N-（3-芳基）丙基丙氨酸残基的关键前体。
- 解析3,3′-双（苄氧基）-1,1′-双萘-2,2′-二醇的外消旋混合物。
- 通过一锅法合成同时包含酰胺和酰亚胺官能团的混合三肽模拟物。
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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)
Convenient synthesis and efficient resolution of 3, 3′-bis (benzyloxy)-1, 1′-binaphthalene-2, 2′-diol
Tsubaki K, et al.
Tetrahedron Asymmetry, 14(10), 1393-1396 (2003)
Synthesis of N-(3-arylpropyl) amino acid derivatives by sonogashira types of reaction in aqueous media
Lopez-Deber MP, et al.
Organic Letters, 3(18), 2823-2826 (2001)
A facile one pot route for the synthesis of imide tethered peptidomimetics
Panduranga V, et al.
Organic & Biomolecular Chemistry, 14(2), 556-563 (2016)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 15380-100G | 04061832641355 |
| 15380-25G | 04061838741103 |
| 15380-5G | 04061838741110 |