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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)-

Butanamide, N-(3-ethoxypropyl)-2,4-dihydroxy-3,3-dimethyl-

CCOCCCNC(=O)C(C(CO)(C)C)O Request for Quotation
Chemical Name: Butanamide, N-(3-ethoxypropyl)-2,4-dihydroxy-3,3-dimethyl-
CAS Number: 667-84-5
Product Number: AG00FA3C(AGN-PC-05W66M)
Synonyms:
MDL No:
Molecular Formula: C11H23NO4
Molecular Weight: 233.30462

Identification/Properties

Computed Properties
Molecular Weight:
233.308g/mol
XLogP3:
0
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
8
Exact Mass:
233.163g/mol
Monoisotopic Mass:
233.163g/mol
Topological Polar Surface Area:
78.8A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
206
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


DL-Ethyl-panthenol, also known as DL-Panthenyl ethyl ether, is a versatile compound that finds numerous applications in chemical synthesis. Due to its structural characteristics, DL-Ethyl-panthenol can serve as a valuable intermediate in the production of various chemicals and pharmaceuticals. In chemical synthesis, DL-Ethyl-panthenol can be utilized as a building block to create more complex molecules through various reactions such as esterification, acylation, or oxidation. Its ethyl and panthenol moieties provide unique reactivity and functionality that can be leveraged to introduce specific chemical groups or modify existing structures. Additionally, DL-Ethyl-panthenol's ability to act as a chiral molecule makes it particularly useful in asymmetric synthesis processes, where the stereochemistry of the final product is crucial. By incorporating DL-Ethyl-panthenol into synthesis routes, chemists can control the stereochemical outcome of reactions and produce enantiomerically pure compounds for various applications.Overall, DL-Ethyl-panthenol's role in chemical synthesis underscores its importance as a versatile building block in the creation of diverse molecules with tailored properties and functionalities. Its applications extend across industries, including pharmaceuticals, cosmetics, and materials science, highlighting its value in driving innovation and advancement in the field of chemistry.