Interesting facts
Interesting Facts about But-2-yne-1,4-diol
But-2-yne-1,4-diol is a fascinating compound that is gaining recognition in various fields, particularly in organic chemistry and materials science. Here are some compelling insights about this compound:
- Structure and Isomerism: But-2-yne-1,4-diol features a unique alkyne linkage with two hydroxyl groups, making it a diol. Its structure allows for isomerism, which can lead to different properties and reactivity.
- Reactivity: The presence of both alkyne and hydroxyl functional groups contributes to its reactivity in various organic reactions. This versatility can be utilized in synthetic applications to build more complex molecules.
- Synthesis: This compound can be synthesized through several methods, one of which involves the hydroboration-oxidation of alkynes. Such pathways make it an interesting target in synthetic organic chemistry.
- Applications: But-2-yne-1,4-diol has potential applications in the production of polymers and other materials. Its diol groups can serve as reactive sites for polymerization, opening up possibilities for novel material properties.
- Biological Relevance: Compounds like but-2-yne-1,4-diol can sometimes show unique biological activities, paving the way for exploration in pharmaceuticals and biochemistry.
As chemists delve deeper into the properties and applications of but-2-yne-1,4-diol, it is clear that this compound is much more than just a simple alkyne. Its ability to participate in diverse chemical reactions makes it a valuable subject of study in the chemical sciences.
Synonyms
2-Butyne-1,4-diol
110-65-6
But-2-yne-1,4-diol
Butynediol
1,4-Dihydroxy-2-butyne
1,4-BUTYNEDIOL
Bis(hydroxymethyl)acetylene
2-Butynediol
2-Butin-1,4-diol
1,4-Butinodiol
Butynediol-1,4
1,4-Butynediol (VAN)
Butynediol-1,4 [French]
1,4-Butinodiol [Spanish]
1,4-Dimethoxyacetylene
DTXSID4021921
HSDB 2004
NSC 834
UNII-AXH202FPQM
EINECS 203-788-6
2-Butin-1,4-diol [Czechoslovakia]
UN2716
BRN 1071237
CHEBI:16413
2-butyn-1,4-diol
AI3-61467
NSC-834
1,2-Dimethoxyacetylene
AXH202FPQM
DTXCID901921
1,4-BUTYNEDIOL [HSDB]
EC 203-788-6
4-01-00-02687 (Beilstein Handbook Reference)
UN 2716
Butynediol-1,4 (French)
Agrisynth B3D
1,4-Butinodiol (Spanish)
2-Butin-1,4-diol (Czechoslovakia)
CAS-110-65-6
2-Butin-1,4-diol [Czech]
But-2-in-1,4-diol
butindiol
butynediols
2Butynediol
1,4Butinodiol
1,4Butynediol
Butynediol1,4
2Butyne1,4diol
But2yne1,4diol
2Butin1,4diol
MFCD00002915
1,4Dihydroxy2butyne
2-butyne-l,4-diol
but-2-yne-1,4diol
1,4Butynediol (VAN)
1,4Dihydroxy-2-butyne
2-butyne-1,4-di-ol
2-Butyne-1, 4-diol
WLN: Q2UU2Q
1,4-BUTYNE GLYCOL
1,2-Dihydroxydimethylacetylene
NSC834
2-Butyne-1,4-diol, 99%
CHEMBL3187551
CHEBI:22970
Tox21_201284
Tox21_302875
STL185542
AKOS000118736
NCGC00249014-01
NCGC00256535-01
NCGC00258836-01
1,4-Butynediol [UN2716] [Poison]
B0749
NS00009569
EN300-19323
Butynediol 1,4-Butynediol 2-Butyne-1,4-diol
C02497
E78871
Q209328
F0001-0223
1,4-Butynediol; 1,4-Dihydroxy-2-butyne; 2-Butynediol; Bis(hydroxymethyl)acetylene; Butynediol; NSC 834
Solubility of But-2-yne-1,4-diol
But-2-yne-1,4-diol is an intriguing compound with unique solubility characteristics. Understanding its solubility can help predict its behavior in various chemical environments. Here are some key points to consider:
In conclusion, the solubility of but-2-yne-1,4-diol is primarily dependent on the solvent environment, showcasing a typical example of the principle “like dissolves like.” Its ability to interact with polar solvents illustrates its versatile nature in chemical applications.