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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)-

1,2-Propanediol, 3-ethoxy-

CCOCC(CO)O Request for Quotation
Chemical Name: 1,2-Propanediol, 3-ethoxy-
CAS Number: 1874-62-0
Product Number: AG00387H(AGN-PC-0JM0KU)
Synonyms:
MDL No:
Molecular Formula: C5H12O3
Molecular Weight: 120.1470

Identification/Properties

Computed Properties
Molecular Weight:
120.148g/mol
XLogP3:
-0.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
120.079g/mol
Monoisotopic Mass:
120.079g/mol
Topological Polar Surface Area:
49.7A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
46.9
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Ethoxy-1,2-propanediol, also known as ethylglycerol, is a versatile chemical compound widely utilized in chemical synthesis for various applications. In organic synthesis, it serves as a valuable building block in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Due to its unique chemical structure, 3-Ethoxy-1,2-propanediol can undergo various reactions such as esterification, etherification, and oxidation to yield a wide range of derivatives with different functionalities. Its ethoxy group provides a reactive site for further modification, making it a crucial intermediate in the synthesis of complex organic molecules. Additionally, 3-Ethoxy-1,2-propanediol can act as a solvent or cosolvent in organic reactions, aiding in the dissolution and mixing of reactants to facilitate the desired chemical transformations. Its role as a solvent also extends to the formulation of various products in industries such as cosmetics, personal care, and pharmaceuticals. Overall, the application of 3-Ethoxy-1,2-propanediol in chemical synthesis underscores its importance in enabling the efficient and controlled production of diverse chemical compounds with valuable properties.