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2-Butynoic acid

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2-Butynoic acid Basic information

Product Name:
2-Butynoic acid
Synonyms:
  • 1-Propynecarboxylic acid
  • 3-Methylpropiolic acid
  • 2-BUTYNOIC ACID
  • BUT-2-YNOIC ACID
  • TETROLIC ACID
  • 2-Butynoicacid,98%
  • 2-BUTYNOIC ACID 98%
  • Methylacetylenecarboxylic acid
CAS:
590-93-2
MF:
C4H4O2
MW:
84.07
EINECS:
209-695-7
Product Categories:
  • API
  • Organic Building Blocks
  • Building Blocks
  • C1 to C5
  • Carbonyl Compounds
  • Carboxylic Acids
  • Acetylenes
  • Acetylenic Carboxylic Acids & Their Derivatives
  • Chemical Synthesis
Mol File:
590-93-2.mol
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2-Butynoic acid Chemical Properties

Melting point:
78-80 °C (lit.)
Boiling point:
200-203°C
Density 
0,9641 g/cm3
refractive index 
1.3918 (estimate)
Flash point:
200-203°C
storage temp. 
Sealed in dry,2-8°C
solubility 
water: soluble50mg/mL, clear to very slightly hazy, colorless to very faintly yellow
form 
Powder
pka
2.62(at 25℃)
color 
White to yellow
Water Solubility 
Soluble in water. Slightly soluble in methanol and chloroform.
BRN 
1740205
InChIKey
LUEHNHVFDCZTGL-UHFFFAOYSA-N
CAS DataBase Reference
590-93-2(CAS DataBase Reference)
NIST Chemistry Reference
2-Butynoic acid(590-93-2)
EPA Substance Registry System
2-Butynoic acid (590-93-2)
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Safety Information

Hazard Codes 
C
Risk Statements 
34-20/21/22
Safety Statements 
26-27-36/37/39-45
RIDADR 
UN 3261 8/PG 2
WGK Germany 
3
TSCA 
Yes
HazardClass 
8
PackingGroup 
II
HS Code 
29161900

MSDS

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2-Butynoic acid Usage And Synthesis

Chemical Properties

white to yellow powder

Uses

Synthon employed in a variety of reactions, including cycloacylation of phenols to flavones and chromones,1 and cyclization to γ-butyrolactones.2

Uses

2-Butynoic acid is used as an intermediate in organic synthesis and pharmaceuticals. It is used as a synthon in various reactions, which includes cylcoalkylation of phenols to flavones and chromones. It is involved in the cyclization of gamma-butyrolactones. It is also used in the synthesis of Z-trisubstituted olefins through μ-alkylation. It plays an important role in the preparation of chirally pure 1,2,3,4-tetrahydroisoquinoline analogs, which finds application as anti-cancer agents.

General Description

The rotational spectrum of 2-butynoic acid was measured by pulsed supersonic-jet Fourier transform microwave spectroscopy.

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