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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)-

Propane, 1,1,3-triethoxy-

CCOCCC(OCC)OCC Request for Quotation
Chemical Name: Propane, 1,1,3-triethoxy-
CAS Number: 7789-92-6
Product Number: AG003AZE(AGN-PC-0JKHQR)
Synonyms:
MDL No:
Molecular Formula: C9H20O3
Molecular Weight: 176.2533

Identification/Properties

Properties
BP:
184-186°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
176.256g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
8
Exact Mass:
176.141g/mol
Monoisotopic Mass:
176.141g/mol
Topological Polar Surface Area:
27.7A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
79.8
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

GHS Pictogram:
Signal Word:
Danger
UN#:
3271
Hazard Statements:
H226-H302
Precautionary Statements:
P305+P351+P338
Class:
3
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Ethoxypropionaldehyde diethyl acetal is a versatile compound commonly used in chemical synthesis for its unique properties and reactivity. This acetal serves as a valuable building block for various organic reactions, particularly in the formation of complex molecules and pharmaceutical intermediates. Its application in the Horner-Wadsworth-Emmons reaction allows for the efficient and selective synthesis of various olefinic compounds, which are commonly found in pharmaceuticals, agrochemicals, and materials science. Additionally, 3-Ethoxypropionaldehyde diethyl acetal can be used in the production of fragrances and flavor compounds through its involvement in the creation of cyclic and acyclic ethers.Furthermore, this compound serves as a protecting group for aldehydes in organic synthesis, enabling chemists to selectively modify specific functional groups without affecting others. Its stability under a variety of reaction conditions makes it an ideal choice for safeguarding aldehyde functionalities during complex synthetic sequences.Overall, the versatile nature and reactivity of 3-Ethoxypropionaldehyde diethyl acetal make it a valuable tool in the hands of synthetic chemists for the streamlined and efficient construction of diverse organic molecules.