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About This Item
Linear Formula:
CH2=CHCH2COOH
CAS Number:
Molecular Weight:
86.09
Beilstein:
1699159
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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
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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.
Signal Word
Danger
Hazard Statements
Precautionary Statements
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 Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Polymer Preprints (American Chemical Society, Division of Polymer Chemistry), 51(1), 399-399 (2010)
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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
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