Merck
CN

541397

Sigma-Aldrich

10-溴癸酸

95%

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线性分子式:
Br(CH2)9CO2H
CAS号:
分子量:
251.16
MDL编号:
PubChem化学物质编号:

检测方案

95%

反应适用性

reagent type: linker

mp

38-41 °C (lit.)

官能团

bromo
carboxylic acid

SMILES字符串

OC(CCCCCCCCCBr)=O

InChI

1S/C10H19BrO2/c11-9-7-5-3-1-2-4-6-8-10(12)13/h1-9H2,(H,12,13)

InChI key

PGVRSPIEZYGOAD-UHFFFAOYSA-N

一般描述

10-Bromodecanoic acid can be prepared from 10-bromodecanol via oxidation.

应用

10-Bromodecanoic acid may be employed as an alkylcarboxylate chain source in the preparation of alkylcarboxylate-grafted polyethylenimine. It may also be used in the synthesis of :
  • 10-(methylsulfinyl)decanoic acid
  • 10-cyanodecanoic acid
  • (10-oxo-10-(4-(3-thioxo-3H-1,2-dithiol-5-yl)phenoxy)-decyl)triphenylphosphonium bromide
  • 11-thiastearic acid

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)

法规信息

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The synthesis and functional evaluation of a mitochondria-targeted hydrogen sulfide donor,(10-oxo-10-(4-(3-thioxo-3 h-1, 2-dithiol-5-yl) phenoxy) decyl) triphenylphosphonium bromide (Ap39).
Le Trionnaire S, et al.
MedChemComm, 5(6), 728-736 (2014)
Fatemeh Soltani et al.
Artificial cells, nanomedicine, and biotechnology, 45(7), 1356-1362 (2016-11-01)
Poor water solubility of hydrophobic drugs is one of the major problems in pharmaceutical sciences. Herein, in order to address the poor solubility of crocetin, the 30% of primary amines of PAMAM G4 and PPI G4 were alkylated and evaluated
Reza K Oskuee et al.
The journal of gene medicine, 11(10), 921-932 (2009-07-28)
Various strategies have been examined to improve both transfection efficiency and cytotoxicity of polyethylenimine (PEI), a widely used polycationic nonviral gene vector. In the present study, we sought to improve PEI transfection efficiency by combining the osmotic burst mechanism for
M D Rahman et al.
Journal of medicinal chemistry, 31(8), 1656-1659 (1988-08-01)
A variety of analogues of stearic acid in which one of the methylene groups was replaced by a sulfur atom were examined as inhibitors of growth and fatty acid biosynthesis in the trypanosomatid protozoan Crithidia fasciculata. The 8-, 9-, 10-
Sara Ayatollahi et al.
The international journal of biochemistry & cell biology, 92, 210-217 (2017-10-17)
RNAi-based gene therapy has been recently considered as a promising approach against cancer. Targeted delivery of drug, gene or therapeutic RNAi-based systems to tumor cells is one of the important issues in order to reduce side effects on normal cells.

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