W424401
2-甲基哌啶
98%
别名:
α-甲基哌啶, 2-哌可啉, NSC 31047, NSC 462
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关于此项目
经验公式（希尔记法）:
C6H13N
化学文摘社编号:
分子量:
99.17
FEMA编号:
4244
Beilstein:
79804
EC 号:
MDL编号:
UNSPSC代码:
12164502
PubChem化学物质编号:
Flavis编号:
14.133
生物来源
synthetic
方案
98%
折射率
n20/D 1.445 (lit.)
沸点
118-119 °C/753 mmHg (lit.)
密度
0.844 g/mL at 25 °C (lit.)
应用
flavors and fragrances
文件
see Safety & Documentation for available documents
食品过敏原
no known allergens
性状检查
fishy
SMILES字符串
CC1CCCCN1
InChI
1S/C6H13N/c1-6-4-2-3-5-7-6/h6-7H,2-5H2,1H3
InChI key
NNWUEBIEOFQMSS-UHFFFAOYSA-N
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警示用语：
Danger
危险分类
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B
储存分类代码
3 - Flammable liquids
WGK
WGK 3
闪点(°F)
50.0 °F - closed cup
闪点(°C)
10 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Efficient solid-phase synthesis of sulfotyrosine peptides using a sulfate protecting-group strategy.
Ahmed M Ali et al.
Angewandte Chemie (International ed. in English), 48(11), 2024-2026 (2009-02-05)
Double protection: Efficient Fmoc-based solid-phase synthesis (SPPS) of sulfotyrosine (sY) peptides is achieved by incorporating the sY residue(s) as a dichlorovinyl-protected (DCV) sulfodiester(s) and using 2-methylpiperidine for Fmoc removal. After removal of the other protecting groups, the DCV group could
J W Sloan et al.
Journal of medicinal chemistry, 28(9), 1245-1251 (1985-09-01)
Previous studies have shown that (+/-)-[3H]nicotine binds to multiple sites in the rat brain P2 preparation. Using a series of pyridine, piperidine and pyrrolidine analogues, the present studies identified drugs with specificity for a separate up-regulatory site that increases the
Yusuf Erdogdu et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 74(1), 162-167 (2009-07-04)
The experimental and theoretical vibrational spectra of 2 and 3-methylpiperidine (abbreviated as 2-MP and 3-MP) were studied. The FT-Infrared spectra of 2-MP and 3-MP molecules were recorded in the liquid phase. The structural and spectroscopic analysis of the title molecules
J W Sloan et al.
Life sciences, 37(15), 1367-1372 (1985-10-14)
(+/-)-2-Methylpiperidine has a high degree of specificity in enhancing the binding of (-)-[3H]nicotine in the rat brain P2 preparation. (-)- and (+)-2-Methylpiperidine have been resolved. The (+) but not the (-) isomer increased the binding of (-)-[3H]nicotine. The two isomers
W R Martin et al.
Pharmacology, biochemistry, and behavior, 29(4), 725-731 (1988-04-01)
The effects of ethylketazocine (EKC) administered intraperitoneally and the nicotinic ligands (-)- and (+)-nicotine, (-)-cytisine, (-)-lobeline, and (+)-2-methylpiperidine administered into the 4th ventricle on the latency of the thermally evoked withdrawal reflex of the decerebrate rat were investigated. EKC administered
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