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10 G
¥197.47
50 G
¥1,668.12
About This Item
经验公式（希尔记法）:
C7H15N
CAS Number:
分子量:
113.20
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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方案
≥99%
表单
liquid
折射率
n20/D 1.4454 (lit.)
沸点
144 °C (lit.)
密度
0.853 g/mL at 25 °C (lit.)
SMILES字符串
CC1CNCC(C)C1
InChI
1S/C7H15N/c1-6-3-7(2)5-8-4-6/h6-8H,3-5H2,1-2H3
InChI key
IDWRJRPUIXRFRX-UHFFFAOYSA-N
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此商品 | T9299 | 280992 | 808388 |
|---|---|---|---|
| Quality Level 100 | Quality Level 200 | Quality Level 100 | Quality Level 200 |
| mp 295 °C (dec.) (lit.) | mp - | mp 165-170 °C (dec.) (lit.) | mp 119-122 °C |
| form powder | form powder | form solid | form solid |
| grade technical grade | grade - | grade - | grade - |
应用
3,5-Dimethylpiperidine was used to investigate the influence of substituents on heterocyclic piperidine as acid corrosion inhibitors for iron[1]. It was used in the synthesis of pure phase ZSM-11 using extremely dense gels with minimal water contents[2].
Reactant for synthesis of:
Substituted bisphenol A derivatives as β-amyloid peptide aggregation inhibitors
MMP-13 selective isonipecotamide α-sulfone hydroxamates
Gem-diamines for active organocatalysts for biodiesel production
Benzimidazole inhibitors of the antigen receptor-mediated NF-κB
Reactant for Mannich reactions to form Ru(II) complexes
Substituted bisphenol A derivatives as β-amyloid peptide aggregation inhibitors
MMP-13 selective isonipecotamide α-sulfone hydroxamates
Gem-diamines for active organocatalysts for biodiesel production
Benzimidazole inhibitors of the antigen receptor-mediated NF-κB
Reactant for Mannich reactions to form Ru(II) complexes
警示用语：
Warning
危险分类
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
3 - Flammable liquids
WGK
WGK 3
闪点(°F)
91.4 °F - closed cup
闪点(°C)
33 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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