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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-Propanol, 2,2-dimethyl-3-(methylamino)-

OCC(CNC)(C)C Request for Quotation
Chemical Name: 1-Propanol, 2,2-dimethyl-3-(methylamino)-
CAS Number: 16047-86-2
Product Number: AG001RYC(AGN-PC-001DHN)
Synonyms:
MDL No:
Molecular Formula: C6H15NO
Molecular Weight: 117.1894

Identification/Properties

Computed Properties
Molecular Weight:
117.192g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
117.115g/mol
Monoisotopic Mass:
117.115g/mol
Topological Polar Surface Area:
32.3A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
61.5
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:
Warning
UN#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Known for its versatile applications in chemical synthesis, 2,2-Dimethyl-3-(methylamino)propan-1-ol offers a wide range of possibilities in the field of chemistry. This compound serves as a valuable building block in the creation of various organic molecules due to its unique molecular structure. With its multiple functional groups, including a tertiary amine and a hydroxyl group, this compound is utilized in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Through strategic chemical transformations, 2,2-Dimethyl-3-(methylamino)propan-1-ol plays a crucial role in the development of complex organic compounds, making it an indispensable asset in modern chemical research and development.