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Merck

80645

Sigma-Aldrich

哌啶 溶液

suitable for peptide synthesis, 20% in DMF

别名:

Azacyclohexane, Cyclopentimine, Hexahydropyridine, Pentamethyleneimine

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500 ML
$268.00
2 L
$787.00

About This Item

经验公式(希尔记法):
C5H11N
CAS号:
分子量:
85.15
Beilstein:
1421082
MDL编号:
UNSPSC代码:
12352005
PubChem化学物质编号:
NACRES:
NA.31

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表单

liquid

质量水平

浓度

20% in DMF

杂质

≤0.1% water

折射率

n20/D 1.434

密度

0.930 g/mL at 20 °C

应用

peptide synthesis

SMILES字符串

C1CCNCC1

InChI

1S/C5H11N/c1-2-4-6-5-3-1/h6H,1-5H2

InChI key

NQRYJNQNLNOLGT-UHFFFAOYSA-N

应用


  • 基于氧杂环的靶向强效抗菌和抗肿瘤吡喃类似物:合成和计算研究: 该研究重点介绍了哌啶溶液在新型吡喃类似物合成中的应用,通过先进的化学合成和计算建模技术,展示了其在增强抗菌和抗肿瘤性能方面的用途(El-Wahab et al., 2024)。

  • 杂环胺诱导的蜜蜂喂食威慑和触角反应.: 该研究利用哌啶溶液,考察了杂环胺对蜜蜂的影响,为植物-昆虫相互作用的化学生态学和农业害虫防治的潜在策略提供了有价值的见解 (Larson et al., 2021).

  • 氢氧化钠/哌啶介质的脱硅和磷改性对甲醇-丙烯转化反应的HZSM-5催化剂催化活性的影响。: 该研究使用哌啶溶液来改变HZSM-5催化剂的表面性质,显著提高了其在甲醇-丙烯转化过程中的性能,突出了其在工业催化中的应用(Safaei et al., 2021)。

  • 以酸性H(2)TiF(6)简单处理ERB-P沸石来合成MWW型钛硅酸盐及其在以H(2)O(2)进行的1-己烯液相环氧化反应中的催化性能。: 该研究利用哌啶溶液来合成新型钛硅酸盐材料,探索了其在己烯催化环氧化中的有效性,显示了哌啶促进先进材料合成的潜力(Guo et al., 2020)。

其他说明

销售限制可能适用

警示用语:

Danger

危险分类

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Eye Dam. 1 - Flam. Liq. 3 - Repr. 1B - Skin Corr. 1B

储存分类代码

3 - Flammable liquids

WGK

WGK 2

闪点(°F)

82.4 °F - closed cup

闪点(°C)

28 °C - closed cup

个人防护装备

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

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Carmine Pasquale Cerrato et al.
Journal of materials chemistry. B, 8(47), 10825-10836 (2020-11-12)
Cell-penetrating peptides are a promising therapeutic strategy for a wide variety of degenerative diseases, ageing, and cancer. Among the multitude of cell-penetrating peptides, PepFect14 has been preferentially used in our laboratory for oligonucleotide delivery into cells and in vivo mouse
Xuwang Chen et al.
Bioorganic & medicinal chemistry, 20(12), 3856-3864 (2012-05-18)
A novel series of piperidine-linked amino-triazine derivatives were designed, synthesized and evaluated for in vitro anti-HIV activity as non-nucleoside reverse transcriptase inhibitors on the basis of our previous work. Screening results indicated that most compounds showed excellent activity against wild-type
Total synthesis of (-)-kopsinine by an asymmetric one-pot [n+2+3] cyclization.
Shingo Harada et al.
Chemistry, an Asian journal, 7(10), 2196-2198 (2012-08-22)
P Ricardo Girling et al.
Organic & biomolecular chemistry, 9(9), 3105-3121 (2011-03-11)
A review into the aza-Diels-Alder reaction, mainly concentrating on literature examples that form piperidin-4-ones from the reaction of imines and electron rich dienes or enones, either through a Lewis acidic/Brønsted acid approach or through the use of an organocatalyst. This
Elisabeth T Hennessy et al.
Science (New York, N.Y.), 340(6132), 591-595 (2013-05-04)
The manipulation of traditionally unreactive functional groups is of paramount importance in modern chemical synthesis. We have developed an iron-dipyrrinato catalyst that leverages the reactivity of iron-borne metal-ligand multiple bonds to promote the direct amination of aliphatic C-H bonds. Exposure

实验方案

KitAlysis™ Cu C-N (Buchwald-Hartwig) cross-coupling high-throughput screening kit. Detailed Set-Up User Guide and a downloadable excel file for calculations.

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