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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-Hexanol, 6-(dimethylamino)-

OCCCCCCN(C)C Request for Quotation
Chemical Name: 1-Hexanol, 6-(dimethylamino)-
CAS Number: 1862-07-3
Product Number: AG003MZX(AGN-PC-0JLBQK)
Synonyms:
MDL No:
Molecular Formula: C8H19NO
Molecular Weight: 145.2426

Identification/Properties

Properties
BP:
117 °C / 12mmHg
Storage:
Room Temperature;
Form:
Liquid
Refractive Index:
1.4460-1.4500
Computed Properties
Molecular Weight:
145.246g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
6
Exact Mass:
145.147g/mol
Monoisotopic Mass:
145.147g/mol
Topological Polar Surface Area:
23.5A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
64.3
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:
Danger
UN#:
2735
Hazard Statements:
H302-H314-H412
Precautionary Statements:
P260-P264-P270-P273-P280-P301+P330+P331+P310-P303+P361+P353+P310+P363-P304+P340+P310-P305+P351+P338+P310-P405-P501
Class:
8
Packing Group:
Ⅱ

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 6-(Dimethylamino)hexan-1-ol plays a vital role in chemical synthesis, particularly in the formation of various organic compounds. Its unique structure consisting of a hexane chain with a dimethylamino group and an alcohol functional group allows it to participate in a wide range of chemical reactions.One key application of 6-(Dimethylamino)hexan-1-ol is in the preparation of quaternary ammonium salts. By reacting this compound with an alkyl halide, such as methyl iodide, the dimethylamino group can undergo quaternization to form a quaternary ammonium salt. These salts have diverse uses in organic chemistry, from phase transfer catalysts to intermediates in pharmaceutical synthesis.Additionally, 6-(Dimethylamino)hexan-1-ol can be employed as a chiral auxiliary in asymmetric synthesis. The chiral center present in the alcohol functional group allows for stereoselective reactions, enabling the production of enantiomerically pure compounds. This is especially valuable in the pharmaceutical industry where the efficacy and safety of drugs often depend on the specific stereochemistry of the molecules.Overall, the versatility of 6-(Dimethylamino)hexan-1-ol makes it a valuable building block in chemical synthesis, enabling the creation of complex organic molecules with diverse applications in various industries.