541397
10-溴癸酸
95%
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关于此项目
线性分子式:
Br(CH2)9CO2H
CAS Number:
分子量:
251.16
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
质量水平
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
新产品
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.
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)
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.
Journal of biomaterials applications, 30(5), 632-648 (2015-08-13)
The applications of polyamidoamine (PAMAM) dendrimers have attracted much attention in biomedicine specially non-viral gene delivery because of thier unique characteristics including hyperbranching, multivalency, and well-defined uniform globular three-dimensional structures. In the current study, in order to enhance the transfection
P Lu et al.
Archives of biochemistry and biophysics, 337(1), 1-7 (1997-01-01)
A series of omega-substituted fatty acids with potential heme-coordinating groups was synthesized as inhibitors of lauric acid omega-hydroxylation. The compounds were evaluated using liver microsomes from clofibrate (CF)-induced rats and an engineered expressed CYP4A1-derived fusion protein called f4A1. omega-Imidazolyl-decanoic acid
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