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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-Propanol, 1-[(2-hydroxyethyl)amino]-

OCCNCC(O)C Request for Quotation
Chemical Name: 2-Propanol, 1-[(2-hydroxyethyl)amino]-
CAS Number: 6579-55-1
Product Number: AG006OGA(AGN-PC-0JM2WB)
Synonyms:
MDL No:
Molecular Formula: C5H13NO2
Molecular Weight: 119.1622

Identification/Properties

Properties
BP:
248.7°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
119.164g/mol
XLogP3:
-1.1
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
119.095g/mol
Monoisotopic Mass:
119.095g/mol
Topological Polar Surface Area:
52.5A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
49.7
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-((2-Hydroxyethyl)amino)propan-2-ol, also known as $name$, is a versatile compound widely used in chemical synthesis processes. One of its key applications is as a multi-functional building block in the production of various organic compounds. Due to its unique structure, $name$ serves as an important intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals.In chemical synthesis, $name$ can act as a bifunctional reagent, enabling the formation of complex molecular structures through versatile reactions. Its hydroxyl and amino groups make it a valuable starting material for the synthesis of diverse compounds. Additionally, the presence of the hydroxyethyl moiety provides opportunities for selective derivatization and modification, allowing chemists to fine-tune the properties of the final products.Furthermore, the use of $name$ in chemical synthesis offers advantages such as ease of handling, compatibility with a wide range of reaction conditions, and the ability to participate in various types of organic transformations. Its role as a key building block makes it an essential component in the toolbox of synthetic chemists seeking to access structurally diverse molecules for pharmaceutical, agrochemical, and material science applications.