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この商品について
実験式(ヒル表記法):
C6H11NO2
CAS番号:
分子量:
129.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
222-359-4
Beilstein/REAXYS Number:
112181
MDL number:
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製品名
1-(2-ヒドロキシエチル)-2-ピロリドン, 98%
InChI key
WDQFELCEOPFLCZ-UHFFFAOYSA-N
InChI
1S/C6H11NO2/c8-5-4-7-3-1-2-6(7)9/h8H,1-5H2
SMILES string
OCCN1CCCC1=O
assay
98%
form
liquid
refractive index
n20/D 1.496 (lit.)
bp
140-142 °C/3 mmHg (lit.)
density
1.143 g/mL at 25 °C (lit.)
functional group
hydroxyl
Quality Level
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関連するカテゴリー
Application
1-(2-Hydroxyethyl)-2-pyrrolidone (HEP) can be used as a starting material for the preparation of chemical intermediates such as 1-vinylpyrrolidinone [1], 1-[2-(diethylamino)ethyl]-2-pyrrolidinone [2], 1-(2-bromoethyl)-2-pyrrolidinone.[3]
It can also be used as a building block in the synthesis of hexakis[2-(2-oxo-1-pyrrolidinyl)ethoxy]cyclotriphosphazene by a nucleophilic substitution reaction with hexachlorocyclotriphosphazene.[4]
It can also be used as a building block in the synthesis of hexakis[2-(2-oxo-1-pyrrolidinyl)ethoxy]cyclotriphosphazene by a nucleophilic substitution reaction with hexachlorocyclotriphosphazene.[4]
1-(2-Hydroxyethyl)-2-pyrrolidone may be used in chemical synthesis.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
保管分類
10 - Combustible liquids
wgk
WGK 2
flash_point_f
212.0 °F - closed cup
flash_point_c
100 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Development of a new production process for N-vinyl-2-pyrrolidone
Shimasaki Y, et al.
Bulletin of the Chemical Society of Japan, 81(4), 449-459 (2008)
Amination of aliphatic alcohols and diols with an iridium pincer catalyst
Andrushko N, et al.
ChemCatChem, 2(6), 640-643 (2010)
Synthesis and radioprotective properties of some 2-pyrrolidone derivatives
Lisina NI, et al.
Pharmaceutical Chemistry Journal, 22(6), 472-476 (1988)
Synthesis and Characterization of Hexakis [2-(2-oxo-1-pyrrolidinyl) Cyclotriphosphazene][J]
Yuefan Y, et al.
Chemistry (Weinheim An Der Bergstrasse, Germany), 7(6), 472-476 (2007)
Matthew J Lacey et al.
ChemSusChem, 10(13), 2758-2766 (2017-05-26)
We report here a water-based functional binder framework for the lithium-sulfur battery systems, based on the general combination of a polyether and an amide-containing polymer. These binders are applied to positive electrodes optimised towards high-energy electrochemical performance based only on
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