162663
DL -2-氨基丁酸
99%, for peptide synthesis, ReagentPlus®
别名:
AABA, Homoalanine, alpha-amino-n-butyric acid
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关于此项目
线性分子式:
C2H5CH(NH2)CO2H
化学文摘社编号:
分子量:
103.12
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352116
EC Number:
220-616-5
MDL number:
Beilstein/REAXYS Number:
635889
产品名称
DL -2-氨基丁酸, ReagentPlus®, 99%
InChI key
QWCKQJZIFLGMSD-UHFFFAOYSA-N
InChI
1S/C4H9NO2/c1-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)
SMILES string
CCC(N)C(O)=O
product line
ReagentPlus®
assay
99%
form
solid
reaction suitability
reaction type: solution phase peptide synthesis
mp
291 °C (dec.) (lit.)
application(s)
peptide synthesis
Quality Level
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General description
DL-2-氨基丁酸，又称为α-氨基丁酸，常用于液相多肽合成法。
Application
DL-2-氨基丁酸可用于合成2-(2,5-二氧代吡咯烷-1-基)丁酸。
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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)
Design, synthesis, and anticonvulsant activity of new hybrid compounds derived from 2-(2, 5-dioxopyrrolidin-1-yl) propanamides and 2-(2, 5-dioxopyrrolidin-1-yl) butanamides
Journal of Medicinal Chemistry, 58, 5274-5286 (2015)
Ryan J Martinie et al.
Journal of the American Chemical Society, 137(21), 6912-6919 (2015-05-13)
The iron(II)- and 2-(oxo)glutarate-dependent (Fe/2OG) oxygenases catalyze an array of challenging transformations, but how individual members of the enzyme family direct different outcomes is poorly understood. The Fe/2OG halogenase, SyrB2, chlorinates C4 of its native substrate, l-threonine appended to the
Francesco Gasparrini et al.
Journal of the American Chemical Society, 130(2), 522-534 (2007-12-22)
The structure, stability, and reactivity of proton-bound diastereomeric [M x H x A]+ complexes between some amino acid derivatives (A) and several chiral tetra-amide macrocycles (M) have been investigated in the gas phase by ESI-FT-ICR and ESI-ITMS-CID mass spectrometry. The
Cornelia Reimmann et al.
Journal of bacteriology, 186(19), 6367-6373 (2004-09-18)
In Pseudomonas aeruginosa, the antibiotic dihydroaeruginoate (Dha) and the siderophore pyochelin are produced from salicylate and cysteine by a thiotemplate mechanism involving the peptide synthetases PchE and PchF. A thioesterase encoded by the pchC gene was found to be necessary
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
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