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2-PENTYNOIC ACID

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CAS:5963-77-9
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CAS:5963-77-9
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CAS:5963-77-9
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Products Intro: Product Name:2-Pentynoic acid
CAS:5963-77-9
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2-PENTYNOIC ACID manufacturers

  • 2-PENTYNOIC ACID
  • 2-PENTYNOIC ACID pictures
  • $1.00
  • 2019-12-27
  • CAS:5963-77-9
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 200kg
2-PENTYNOIC ACID Basic information
Product Name:2-PENTYNOIC ACID
Synonyms:2-PENTYNOIC ACID;ethylacetylene carboxylic acid;Nsc289567;2-Pentynoic acid 97%;2-PENTYNOIC ACID, 98%2-PENTYNOIC ACID, 98%2-PENTYNOIC ACID, 98%2-PENTYNOIC ACID, 98%;Pent-2-ynoic acid
CAS:5963-77-9
MF:C5H6O2
MW:98.1
EINECS:
Product Categories:C1 to C5Organic Building Blocks;Alkynes;Carbonyl Compounds;Carboxylic Acids;Internal
Mol File:5963-77-9.mol
2-PENTYNOIC ACID Structure
2-PENTYNOIC ACID Chemical Properties
Melting point 47-53 °C
Boiling point 125°C 30mm
density 1.1133 (rough estimate)
refractive index 1.4619
Fp 96 °C
storage temp. 2-8°C
form Solid
pka2.70±0.10(Predicted)
AppearanceWhite to yellow Solid
InChIInChI=1S/C5H6O2/c1-2-3-4-5(6)7/h2H2,1H3,(H,6,7)
InChIKeyMINRDQDGBLQBGD-UHFFFAOYSA-N
SMILESC(O)(=O)C#CCC
Safety Information
Hazard Codes Xn
Risk Statements 34-36/37/38-22
Safety Statements 26-36/37/39-36
RIDADR 3261
WGK Germany 1
HS Code 29161900
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
2-PENTYNOIC ACID Usage And Synthesis
Uses2-Pentynoic Acid is a chemical reagent used in the preparation of various organic molecule. Used in the stereoselective synthesis of vinylstannanes. In addition, it is used in the synthesis of spiroindolines derivatives.
Application2-Pentynoic acid serves as a precursor in coupling with iodobenzene to prepare aryl alkyne carboxylic acids, and reacts with iodobenzene, Na2S·5H2O, and DBU to yield (Z)-3-(phenylthio)pent-2-enoic acid[1][3].
It reacts with morpholine and paraformaldehyde to afford the corresponding product[3].
It serves as a starting material to afford 3,4-dichloro-5-methylfuran-2(5H)-one[2].
References[1] Palani, T., Park, K., Song, K., & Lee, S. (2013). Palladium‐Catalyzed Synthesis of (Z)‐3‐Arylthioacrylic Acids and Thiochromenones. ChemInform, 55 1. https://doi.org/10.1002/CHIN.201337069
[2] Jayaraman, A., Cho, E., Irudayanathan, F. M., Kim, J., & Lee, S. (2018). Metal‐Free Decarboxylative Trichlorination of Alkynyl Carboxylic Acids: Synthesis of Trichloromethyl Ketones. Advanced Synthesis & Catalysis, 360 1, Pages 130-141. https://doi.org/10.1002/adsc.201701116
[3] Park, K., Heo, Y., & Lee, S. Experimental Procedure S2-S12 Spectroscopic Data S12-S47.
Tag:2-PENTYNOIC ACID(5963-77-9) Related Product Information
2-OCTYNOIC ACID METHYL 2-HEPTYNOATE METHYL 2-HEXYNOATE ETHYL 2-HEXYNOATE 2-Pentynoic acid ethyl ester 2-HEXYNOIC ACID ETHYL 2-OCTYNOATE ETHYL 2-HEPTYNOATE 2-HEPTYNOIC ACID ETHYL 2-NONYNOATE METHYL 2-OCTYNOATE 2-PENTYNOIC ACID METHYL 2-NONYNOATE L-Propargylglycine HCL 4-PENTYNOIC ACID D-PROPARGYLGLYCINE DL-PROPARGYLGLYCINE L-Propargylglycine