H10401
环己亚胺
99%
别名:
1-氮杂环庚烷, HMI, 氮杂卓, 过氧氮杂卓, 六氢-1H-氮杂卓, 高哌啶
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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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-875-9
Beilstein/REAXYS Number:
1084
MDL number:
Assay:
99%
Form:
liquid
InChI
1S/C6H13N/c1-2-4-6-7-5-3-1/h7H,1-6H2
InChI key
ZSIQJIWKELUFRJ-UHFFFAOYSA-N
SMILES string
C1CCCNCC1
vapor pressure
7.4 mmHg ( 21.1 °C)
assay
99%
form
liquid
refractive index
n20/D 1.466 (lit.)
bp
138 °C/749 mmHg (lit.)
density
0.88 g/mL at 25 °C (lit.)
Quality Level
Application
六亚甲基亚胺 (HMI) 可用于制备：
也可用于（−）-巴拉醇、吲哚雌激素、柔红霉素和 (+)-西替地尔的衍生物。
- 沸石催化剂如 MCM-22 和 MCM-49
- SAPO-35，分子筛
- 各种微孔铝硅酸盐和钛硅酸盐
- 有机-无机杂化紫苏叶石
也可用于（−）-巴拉醇、吲哚雌激素、柔红霉素和 (+)-西替地尔的衍生物。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 2 Oral - Acute Tox. 3 Inhalation - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1C - STOT SE 3
target_organs
Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
64.4 °F - closed cup
flash_point_c
18 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Synthesis of zeolite MCM-22 under rotating and static conditions. Microporous and mesoporous materials.
Guray I, et al.
Microporous and Mesoporous Materials : The Official Journal of the International Zeolite Association, 31(3), 241-251 (1999)
Design, synthesis, and preclinical characterization of novel, highly selective indole estrogens.
Miller CP, et al.
Journal of Medicinal Chemistry, 44(11), 1654-1657 (2001)
Zeolite MCM-49: a three-dimensional MCM-22 analogue synthesized by in situ crystallization.
Lawton SL, et al.
The Journal of Physical Chemistry, 100(9), 3788-3798 (1996)
Longle Ma et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 22(50), 18179-18189 (2016-10-07)
Cyclic amines such as pyrrolidine and piperidine are known to undergo condensations with aldehydes to furnish pyrrole and pyridine derivatives, respectively. A combined experimental and computational study provides detailed insights into the mechanism of pyrrole formation. A number of reactive
J R Lundkvist et al.
Journal of medicinal chemistry, 33(12), 3182-3189 (1990-12-01)
A series of conformationally restricted analogues of the partial muscarinic agonist N-methyl-N-(1-methyl-4-pyrrolidino-2-butynyl)acetamide (BM 5; 1) was synthesized. Three of the racemic derivatives were resolved into the enantiomers. The compounds were investigated for muscarinic and antimuscarinic activity in the isolated guinea
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