161667
10-Undecenoyl chloride
97%
동의어(들):
ψ-Undecenoyl chloride, ψ-Undecylenic acid chloride, 10-Hendecenoyl chloride, Undec-10-enoyl chloride
로그인조직 및 계약 가격 보기
모든 사진(2)
About This Item
Linear Formula:
CH2=CH(CH2)8COCl
CAS Number:
Molecular Weight:
202.72
Beilstein:
1635112
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
분석
97%
양식
liquid
refractive index
n20/D 1.454 (lit.)
bp
120-122 °C/10 mmHg (lit.)
density
0.944 g/mL at 25 °C (lit.)
작용기
acyl chloride
allyl
SMILES string
ClC(=O)CCCCCCCCC=C
InChI
1S/C11H19ClO/c1-2-3-4-5-6-7-8-9-10-11(12)13/h2H,1,3-10H2
InChI key
MZFGYVZYLMNXGL-UHFFFAOYSA-N
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애플리케이션
10-Undecenoyl chloride was used as acylating reagent in the synthesis of cellulose ω-carboxyalkanoates and poly(ethylene glycol)–lipid amphiphiles. It was used in synthesis and modification of hyperbranched poly(glycidol).
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point (°F)
199.4 °F
Flash Point (°C)
93 °C
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
이미 열람한 고객
Huan Liu et al.
Small (Weinheim an der Bergstrasse, Germany), 16(44), e2004922-e2004922 (2020-10-09)
For the first time Janus-like films of surface-acylated cellulose nanowhiskers (CNWs) with or without graphene oxide (GO) via one-step evaporation-driven self-assembly process are reported, which have reconstructible time-dependent micro-/nanostructures and asymmetric wettability. The heterogeneous aggregation of CNWs on rough Teflon
Enhancement of the impact strength of cationically cured cycloaliphatic diepoxide by adding hyperbranched poly (glycidol) partially modified with 10-undecenoyl chains.
Flores M, et al.
Eur. Polymer J., 49(6), 1610-1620 (2013)
Kamila Szwed et al.
Journal of separation science, 39(6), 1110-1117 (2016-03-31)
Cyclodextrins and their derivatives are one of the most common and successful chiral selectors. However, there have been few publications about the use of cyclodextrin-modified monoliths. In this study, organic hybrid monoliths were prepared by the immobilization of derivatized β-cyclodextrin
Core crosslinkable polymeric micelles from PEG-lipid amphiphiles as drug carriers.
Tian L, et al.
Journal of Materials Chemistry, 14(14), 2317-2324 (2004)
Xiangtao Meng et al.
Biomacromolecules, 15(1), 177-187 (2013-12-18)
Cross-metathesis has been shown for the first time to be a useful method for the synthesis of polysaccharide derivatives, focusing herein on preparation of cellulose ω-carboxyalkanoates. Commercially available cellulose esters were first acylated with 10-undecenoyl chloride, providing esters with olefin-terminated
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