Ethanol, 2-[(1,1-dimethylethyl)amino]-


Chemical Name: Ethanol, 2-[(1,1-dimethylethyl)amino]-
CAS Number: 4620-70-6
Product Number: AG003F4P(AGN-PC-0D5OOK)
Synonyms:
MDL No:
Molecular Formula: C6H15NO
Molecular Weight: 117.1894

Identification/Properties


Properties
MP:
41-43 °C(lit.)
BP:
176.5°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Refractive Index:
1.4444 (estimate)
Computed Properties
Molecular Weight:
117.192g/mol
XLogP3:
0.4
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:
56
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:
H312-H315
Precautionary Statements:
P280
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



2-(tert-Butylamino)ethanol is a versatile compound commonly used in chemical synthesis as a chiral auxiliary. Its primary application lies in asymmetric synthesis, where it serves as a valuable tool for controlling stereochemistry in organic reactions. By strategically incorporating 2-(tert-Butylamino)ethanol into a reaction scheme, chemists can influence the formation of enantiomerically enriched products, essential in the pharmaceutical and agrochemical industries. Additionally, this compound can play a crucial role in the preparation of various intermediates and complex molecules, showcasing its significance in the realm of modern organic chemistry. With its unique structural features and reactivity, 2-(tert-Butylamino)ethanol has become a sought-after reagent in the hands of synthetic chemists aiming to access specific chiral compounds efficiently.