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Merck
CN

469505

Sigma-Aldrich

(R)-2-(Boc-氨基)-1-丙醇

98%, optical purity ee: 98% (GLC)

别名:

(R)-(+)-2-(叔丁氧羰基氨基)-1-丙醇, N-Boc-D-丙氨醇

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About This Item

线性分子式:
CH3CH[NHCO2C(CH3)3]CH2OH
分子量:
175.23
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:

方案

98%

表单

solid

旋光性

[α]20/D +11°, c = 1 in chloroform

光学纯度

ee: 98% (GLC)

反应适用性

reaction type: Boc solid-phase peptide synthesis

mp

58-61 °C (lit.)

应用

peptide synthesis

SMILES字符串

C[C@H](CO)NC(=O)OC(C)(C)C

InChI

1S/C8H17NO3/c1-6(5-10)9-7(11)12-8(2,3)4/h6,10H,5H2,1-4H3,(H,9,11)/t6-/m1/s1

InChI key

PDAFIZPRSXHMCO-ZCFIWIBFSA-N

应用

用于合成抗血栓 3-哌啶甲酰胺。

储存分类代码

13 - Non Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Anna Said Stålsmeden et al.
Organic & biomolecular chemistry, 18(10), 1957-1967 (2020-02-27)
1,4- and 1,5-Disubstituted triazole amino acid monomers have gained increasing interest among peptidic foldamers, as they are easily prepared via Cu- and Ru-catalyzed click reactions, with the potential for side chain variation. While the latter is key to their applicability
X Zheng et al.
Chirality, 7(2), 90-95 (1995-01-01)
The stereoisomers of alpha,alpha'-bis[3-(N,N-diethylcarbamoyl)-piperidino]-p-xylene (1) were synthesized. Rac ethyl nipecotate was resolved by diastereomeric (-)-D- and (+)-L-tartrate salt formation. The enantiomeric esters were hydrolyzed to the corresponding nipecotic acids, which were then converted into t-BOC derivatives. Treatment of the latter

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