140996
Ethyl crotonate
96%
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
CH3CH=CHCOOC2H5
Molecular Weight:
114.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-808-7
Beilstein/REAXYS Number:
635834
MDL number:
Assay:
96%
Form:
liquid
vapor density
3.9 (vs air)
assay
96%
form
liquid
refractive index
n20/D 1.424 (lit.)
bp
142-143 °C (lit.)
density
0.918 g/mL at 25 °C (lit.)
SMILES string
CCOC(=O)\C=C\C
InChI
1S/C6H10O2/c1-3-5-6(7)8-4-2/h3,5H,4H2,1-2H3/b5-3+
InChI key
ZFDIRQKJPRINOQ-HWKANZROSA-N
General description
Ethyl crotonate on hydroboration yields stereospecifically 2-tritiated 3-hydroxybutyric acid.
Application
Ethyl crotonate was used in chemical-shift imaging during the rapid analysis of multiple samples using multiplex sample NMR. It was used as reagent during the total synthesis of (+/-)-daurichromenic acid.
Still not finding the right product?
Explore all of our products under Ethyl crotonate
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
35.6 °F - closed cup
flash_point_c
2 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
P Willadsen et al.
European journal of biochemistry, 54(1), 247-252 (1975-05-01)
1. A specimen of stereospecifically 2-tritiated 3-hydroxybutyric acid was prepared by hydroboration of ethyl crotonate. It was assumed that the hydroboration reaction took a syn course and hence that (2R,3S) plus (2S,3R)-3-hydroxy[2 minus 3H1]butyric acid was formed after oxidation and
Hongjuan Hu et al.
The Journal of organic chemistry, 69(11), 3782-3786 (2004-05-22)
A modular and concise total synthesis of (+/-)-daurichromenic acid has been accomplished in four steps from ethyl acetoacetate, ethyl crotonate, and trans,trans-farnesal. A series of analogues of this natural product, which has potent anti-HIV activity, were also prepared from ethyl
T Hou et al.
Analytical chemistry, 73(11), 2541-2546 (2001-06-14)
Two improved approaches for the rapid analysis of multiple samples using multiplex sample NMR are described. In the first approach, frequency-selective 90 degrees radio frequency pulses and large pulsed field gradients are applied to excite and detect multiple samples in
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 140996-100ML | 04061836691110 |