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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-diethylaminopropan-2-ol

CCN(CC(O)C)CC Request for Quotation
Chemical Name: 1-diethylaminopropan-2-ol
CAS Number: 4402-32-8
Product Number: AG003E9T(AGN-PC-0JM19G)
Synonyms:
MDL No:
Molecular Formula: C7H17NO
Molecular Weight: 131.2160

Identification/Properties

Properties
BP:
55-59°C at 13 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
131.219g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
131.131g/mol
Monoisotopic Mass:
131.131g/mol
Topological Polar Surface Area:
23.5A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
61.9
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(Diethylamino)propan-2-ol is a versatile compound widely utilized in chemical synthesis as a valuable building block. With its unique structure, this compound serves as an important intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. In chemical synthesis, 1-(Diethylamino)propan-2-ol is commonly employed as a chiral auxiliary, facilitating the asymmetric synthesis of complex molecules. Its presence allows for the control of stereochemistry during the formation of carbon-carbon and carbon-heteroatom bonds, leading to enantiopure products with high selectivity.Furthermore, this compound is utilized as a reagent in the preparation of functionalized derivatives through a variety of reactions such as acylation, alkylation, and oxidation. Its hydroxyl and amino groups enable it to participate in diverse transformations, expanding its utility in organic synthesis.Overall, 1-(Diethylamino)propan-2-ol plays a crucial role in the development of new compounds with enhanced biological activity, making it an indispensable component in the repertoire of synthetic chemists seeking to create innovative molecules for various applications.