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主要文件

47624

Sigma-Aldrich

Fmoc-Lys(Boc)-OH

≥98.0% (HPLC), for peptide synthesis

别名:

Nα-芴甲氧羰基-Nε-叔丁氧羰基-L-赖氨酸

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1 L
CN¥945.70
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预计发货时间July 07, 2025详情


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1 L
CN¥945.70
2.5 L
CN¥2,007.65
4 L
CN¥3,258.68

About This Item

经验公式(希尔记法):
C26H32N2O6
CAS号:
分子量:
468.54
Beilstein:
4217767
EC 号:
MDL编号:
UNSPSC代码:
12352209
eCl@ss:
32160406
PubChem化学物质编号:
NACRES:
NA.26

CN¥945.70


预计发货时间July 07, 2025详情


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产品名称

Fmoc-Lys(Boc)-OH, ≥98.0% (HPLC)

质量水平

方案

≥98.0% (HPLC)

表单

solid

旋光性

[α]20/D −12±1°, c = 1% in DMF

反应适用性

reaction type: Fmoc solid-phase peptide synthesis

应用

peptide synthesis

官能团

Boc
Fmoc

储存温度

2-8°C

SMILES字符串

CC(C)(C)OC(=O)NCCCC[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O

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technique(s)

gas chromatography (GC): suitable

technique(s)

-

technique(s)

-

technique(s)

-

Quality Level

100

Quality Level

300

Quality Level

300

Quality Level

200

form

liquid

form

liquid

form

liquid

form

liquid

mp

<-80 °C

mp

-

mp

<-80 °C

mp

-

expl. lim.

0.8-7.4 % (v/v)

expl. lim.

1.2-7.5 % (v/v)

expl. lim.

1.0-7.4 % (v/v)

expl. lim.

1.3-7.8 % (v/v)

bp

40-60 °C/1013 hPa

bp

30-50 °C/1013 hPa

bp

36-83 °C/1013 hPa

bp

<40 °C/1013 hPa

一般描述

Fmoc-Lys(Boc)-OH 是一种氨基酸衍生物,用于Fmoc固相合成多肽的试剂。[1][2]

应用

Fmoc-Lys(Boc)-OH可用于:
  • 通过与甲基苯甲胺(MBHA)树脂偶联固相合成五取代的二氢咪唑基丁基二氢咪唑-3-盐。[3]
  • 基于Fmoc多肽合成线性嵌插剂双萘四酰亚二胺[4]
  • 合成ε-Boc-ε-(3,5-双-三氟甲基-苄基)-α-Fmoc-L-赖氨酸,可用作基于19F NMR的筛选工具。[5]

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

  • 技术规格说明书

  • 历史批次信息供参考:

    分析证书(COA)

    Lot/Batch Number

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    Marta Kulik et al.
    Biochimie, 138, 32-42 (2017-04-12)
    A fragment of 23S ribosomal RNA (nucleotides 1906-1924 in E. coli), termed Helix 69, forms a hairpin that is essential for ribosome function. Helix 69 forms a conformationally flexible inter-subunit connection with helix 44 of 16S ribosomal RNA, and the nucleotide
    Bis-naphthalene diimide exhibiting an effective bis-threading intercalating ability.
    Nojima T, et al.
    Nucleic Acids Symposium Series, 3(1), 123-124 (2003)
    Marine Bacchi et al.
    Protein science : a publication of the Protein Society, 25(12), 2225-2242 (2016-09-28)
    Synthetic biology (or chemical biology) is a growing field to which the chemical synthesis of proteins, particularly enzymes, makes a fundamental contribution. However, the chemical synthesis of catalytically active proteins (enzymes) remains poorly documented because it is difficult to obtain
    Solid-phase parallel synthesis of substituted dihydroimidazolylbutyl dihydroimidazol-3-ium salts.
    Acharya AN, et al.
    Tetrahedron Letters, 43(7), 1157-1160 (2002)
    Improved synthesis of polyfluorinated l-lysine for 19F NMR-based screening.
    Malgesini B, et al.
    Molecular Diversity, 13(1), 53-56 (2009)

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