134716
3-Butenoic acid
97%
Synonym(s):
Vinylacetic acid
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About This Item
Linear Formula:
CH2=CHCH2COOH
CAS Number:
Molecular Weight:
86.09
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1699159
Assay:
97%
Quality Level
assay
97%
contains
hydroquinone as inhibitor
refractive index
n20/D 1.423 (lit.)
bp
163 °C (lit.)
mp
−39 °C (lit.)
density
1.013 g/mL at 25 °C (lit.)
functional group
allyl, carboxylic acid
storage temp.
2-8°C
SMILES string
OC(=O)CC=C
InChI
1S/C4H6O2/c1-2-3-4(5)6/h2H,1,3H2,(H,5,6)
InChI key
PVEOYINWKBTPIZ-UHFFFAOYSA-N
Application
3-Butenoic acid was used in the synthesis of polyethylene glycolated boltorn coatings. It was used to study the inhibition of the enzyme-catalysed conversion of D-tyrosyl- phenylalanyl-glycine to D-tyrosyl-phenylaline amide by non-peptide carboxylic acids. It was used in preparation of strained nitroso Diels-Aldrer adducts which undergo a domino ROC metathesis in the presence of Ru-carbene catalysts and olefins.
signalword
Danger
Hazard Classifications
Aquatic Chronic 2 - Carc. 2 - Eye Dam. 1 - Muta. 2 - Skin Corr. 1B - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Géraldine Calvet et al.
Organic letters, 9(8), 1485-1488 (2007-03-14)
[reaction: see text] Strained bicyclic 3,6-dihydro-1,2-oxazine is a reactive substrate in domino metathesis with an external alkene. This general transformation leads to isoxazolo[2,3-a]pyridin-7-one, a versatile scaffold combining chemical functions that could be selectively oxidized or reduced. The synthetic relevance of
Meghan E Dunn et al.
The journal of physical chemistry. A, 112(41), 10226-10235 (2008-09-19)
In this study we present the gas-phase vibrational spectrum of vinylacetic acid with a focus on the nu = 1-5 vibrational states of the OH stretching transitions. Cross sections for nu = 1, 2, 4 and 5 of the OH
Lvfeng Zhu et al.
The Journal of organic chemistry, 75(17), 6027-6030 (2010-08-13)
A challenging direct asymmetric hydrogenation of (E)-2-oxo-4-arylbut-3-enoic acids to give 2-hydroxy-4-arylbutanoic acids (85.4-91.8% ee) was achieved with a Ru catalyst based on SunPhos as the chiral ligand. Further investigation of the reaction revealed that partial isomerization of 2-hydroxy-4-arylbutenoic acids was
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 134716-100G | 04061838730213 |
| 134716-25G | 04061838730220 |