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Merck
CN

162663

Sigma-Aldrich

DL -2-氨基丁酸

99%, for peptide synthesis, ReagentPlus®

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别名:
AABA, Homoalanine, alpha-amino-n-butyric acid
线性分子式:
C2H5CH(NH2)CO2H
CAS号:
分子量:
103.12
Beilstein:
635889
EC 号:
MDL编号:
UNSPSC代码:
12352116
PubChem化学物质编号:
NACRES:
NA.22

质量水平

产品线

ReagentPlus®

检测方案

99%

形式

solid

反应适用性

reaction type: solution phase peptide synthesis

mp

291 °C (dec.) (lit.)

应用

peptide synthesis

SMILES字符串

CCC(N)C(O)=O

InChI

1S/C4H9NO2/c1-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)

InChI key

QWCKQJZIFLGMSD-UHFFFAOYSA-N

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一般描述

DL-2-氨基丁酸,又称为α-氨基丁酸,常用于液相多肽合成法。

应用

DL-2-氨基丁酸可用于合成2-(2,5-二氧代吡咯烷-1-基)丁酸。

法律信息

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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Danica P Galonić et al.
Nature chemical biology, 3(2), 113-116 (2007-01-16)
Enzymatic incorporation of a halogen atom is a common feature in the biosyntheses of more than 4,500 natural products. Halogenation of unactivated carbon centers in the biosyntheses of several compounds of nonribosomal peptide origin is carried out by a class
Izumi Kawabata et al.
Nature communications, 3, 722-722 (2012-03-08)
Synaptic remodelling coordinated with dendritic growth is essential for proper development of neural connections. After establishment of synaptic contacts, synaptic junctions are thought to become stationary and provide fixed anchoring points for further dendritic growth. However, the possibility of active

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