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About This Item
经验公式（希尔记法）:
C6H13N
CAS号:
分子量:
99.17
MDL编号:
UNSPSC代码:
12352005
PubChem化学物质编号:
NACRES:
NA.22
推荐产品
质量水平
方案
97%
旋光性
[α]20/D +35°, c = 3.5 in hexane
折射率
n20/D 1.446 (lit.)
沸点
117-121 °C (lit.)
密度
0.823 g/mL at 25 °C (lit.)
SMILES字符串
C[C@H]1CCCCN1
InChI
1S/C6H13N/c1-6-4-2-3-5-7-6/h6-7H,2-5H2,1H3/t6-/m0/s1
InChI key
NNWUEBIEOFQMSS-LURJTMIESA-N
应用
(S)-(+)-2-Methylpiperidine has been used in the preparation of (S)-N-(3-(2-pipecolin-1-yl)propyl)phthalimide by reacting with N-(3-bromopropyl)phthalimide. It may also be used as a starting material in the multi-step synthesis of (2S,6S)-(+)-solenopsin A.
警示用语：
Danger
危险分类
Eye Irrit. 2 - Flam. Liq. 2 - 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)
60.0 °F - closed cup
闪点(°C)
15.56 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Noncyclam Tetraamines Inhibit CXC Chemokine Receptor Type 4 and Target Glioma-Initiating Cells.
Ros-Blanco L, et al.
Journal of Medicinal Chemistry, 55(17), 7560-7570 (2012)
Anodic Cyanation of (-)-N-Phenyl-2-Methylpiperidine: A Short Synthesis of (+)-Solenopsin A and (+)-Isosolenopsin A.
Girard N, et al.
Synthetic Communications, 35(5), 711-723 (2005)
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