所有图片(1)
About This Item
经验公式（希尔记法）:
C8H15N3
CAS号:
分子量:
153.22
Beilstein:
7635759
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
推荐产品
![1,5,7-三氮杂双环 [4.4.0] 癸烯-5-烯 98%](/deepweb/assets/sigmaaldrich/product/structures/171/446/333d560c-cff6-4958-b489-5acfb3057cce/640/333d560c-cff6-4958-b489-5acfb3057cce.png)
![1,8-二氮杂双环[5.4.0]十一碳-7-烯 98%](/deepweb/assets/sigmaaldrich/product/structures/120/564/5b373e23-1624-489c-8efb-692de0f96ffb/640/5b373e23-1624-489c-8efb-692de0f96ffb.png)
![1,4-二叠氮双环[2.2.2]辛烷 ReagentPlus®, ≥99%](/deepweb/assets/sigmaaldrich/product/structures/366/129/a6ff4175-974d-4fac-9038-b35e508ef252/640/a6ff4175-974d-4fac-9038-b35e508ef252.png)
质量水平
方案
98%
表单
liquid
折射率
n20/D 1.537 (lit.)
沸点
75-79 °C/0.1 mmHg (lit.)
密度
1.067 g/mL at 25 °C (lit.)
SMILES字符串
CN1CCCN2CCCN=C12
InChI
1S/C8H15N3/c1-10-5-3-7-11-6-2-4-9-8(10)11/h2-7H2,1H3
InChI key
OEBXWWBYZJNKRK-UHFFFAOYSA-N
正在寻找类似产品? 访问 产品对比指南
一般描述
7-甲基-1,5,7-三氮杂二环[4.4.0]癸-5-烯是一种可溶性胺碱。 它与4-硝基苯基[双(二乙基磺酰基)]甲烷和苯基[双(二乙基磺酰基)]甲烷形成1:1配合物，并且已通过FT-IR、1H NMR和PM5半经验方法研究了它们的结构。 已经研究了7-甲基-1,5,7-三氮杂二环[4.4.0]癸-5-烯对菜籽油与甲醇的酯交换反应的催化性能。
应用
7-甲基-1,5,7-三氮杂二环[4.4.0]癸-5-烯可用于微波促进的、钯催化的与芳基/杂芳基九氟磺酸盐和胺的C-N键形成反应。 它可以作为强碱，用于研究多足配体溶剂、三(氧杂烷基)苯基硅烷和三(氧杂烷基)磷酸酯。
警示用语：
Danger
危险声明
危险分类
Eye Dam. 1 - Skin Corr. 1B
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 3
闪点(°F)
235.4 °F - closed cup
闪点(°C)
113 °C - closed cup
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Rachel E Tundel et al.
The Journal of organic chemistry, 71(1), 430-433 (2006-01-04)
[reaction: see text] Microwave-assisted, palladium-catalyzed C-N bond-forming reactions with aryl/heteroaryl nonaflates and amines using the soluble amine bases DBU (1,8-diazabicyclo[5.4.0]undec-7-ene) or MTBD (7-methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene) and ligands (1-3) resulted in good to excellent yields (71-99%) of arylamines in short reaction times (1-45
Transesterification of vegetable oils: a review.
Schuchardt U, et al.
Journal of the Brazilian Chemical Society, 9(3), 199-210 (1998)
Podand solvents for organic reactions.
Gierczyk B, et al.
Supramolecular Chemistry, 14(6), 497-502 (2002)
Spectroscopic studies of the 1: 1 complexes of 4-nitrophenyl [bis (ethylsulfonyl)] methane and phenyl [bis (ethylsulfonyl)] methane with 7-methyl-1, 5, 7-triazabicyclo [4.4. 0] dec-5-ene and 1, 5, 7-triazabicyclo [4.4. 0] dec-5-ene.
Huczynski A, et al.
Journal of Molecular Structure, 841(1), 133-136 (2007)
Jiun-Min Hsu et al.
PLoS genetics, 10(11), e1004715-e1004715 (2014-11-14)
Neuronal cargos are differentially targeted to either axons or dendrites, and this polarized cargo targeting critically depends on the interaction between microtubules and molecular motors. From a forward mutagenesis screen, we identified a gain-of-function mutation in the C. elegans α-tubulin
商品
The prevalence of organofluorine compounds in industry and drug design necessitates the ability to introduce C–F bonds to molecules.
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门