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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2-Butyne, 1,1-diethoxy-

CCOC(C#CC)OCC Request for Quotation
Chemical Name: 2-Butyne, 1,1-diethoxy-
CAS Number: 2806-97-5
Product Number: AG003GTX(AGN-PC-0JMPNF)
Synonyms:
MDL No:
Molecular Formula: C8H14O2
Molecular Weight: 142.19556

Identification/Properties

Properties
Storage:
Room Temperature;Inert atmosphere;
Computed Properties
Molecular Weight:
142.198g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
142.099g/mol
Monoisotopic Mass:
142.099g/mol
Topological Polar Surface Area:
18.5A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
123
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Butynaldiethylacetal, also known as DEOB, is a versatile compound commonly employed in chemical synthesis as a useful building block. Its unique structure and reactivity make it a valuable tool in organic chemistry for the preparation of various compounds.One of the key applications of 2-Butynaldiethylacetal is in its role as a protective group for aldehydes and ketones. By selectively masking reactive carbonyl groups using DEOB, chemists can prevent unwanted side reactions or achieve specific transformations in complex molecules. The acetal group formed by DEOB is stable under a variety of reaction conditions, allowing for strategic deprotection to unveil the original carbonyl functionality when needed.Furthermore, 2-Butynaldiethylacetal serves as a valuable synthon for the introduction of an alkyne moiety into organic molecules. Through controlled reactions with various nucleophiles or electrophiles, DEOB can be utilized for the synthesis of diverse alkynyl derivatives with potential applications in pharmaceuticals, materials science, and agrochemicals.Overall, the strategic use of 2-Butynaldiethylacetal in chemical synthesis enables chemists to access novel molecular architectures, facilitate complex synthetic pathways, and unlock new opportunities for the development of advanced functional materials.