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2-Benzylamino-2-methyl-1-propanol

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CAS:10250-27-8
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CAS:10250-27-8
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CAS:10250-27-8
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2-Benzylamino-2-methyl-1-propanol Basic information
Uses
Product Name:2-Benzylamino-2-methyl-1-propanol
Synonyms:2-Benzylamino-2-methyl-1-propanol;2-Methyl-2-[(phenylmethyl)amino]-1-propanol;(Benzyl)(2-hydroxy-1,1-dimethylethyl)amine;2-(benzylamino)-2-methyl-1-propanol(SALTDATA: HCl);BMK GLYCIDATE FACTORY;New bmk glycidate powder;2-Benzylamino-2-methyl-1-propano;1-Propanol, 2-methyl-2-[(phenylmethyl)amino]-
CAS:10250-27-8
MF:C11H17NO
MW:179.26
EINECS:202-303-5
Product Categories:intermediate;Chemical Amines;Amines;Aromatics
Mol File:10250-27-8.mol
2-Benzylamino-2-methyl-1-propanol Structure
2-Benzylamino-2-methyl-1-propanol Chemical Properties
Melting point 68-70℃
Boiling point 300.8±17.0 °C(Predicted)
density 1.006±0.06 g/cm3(Predicted)
storage temp. 2-8°C(protect from light)
solubility Chloroform, DMSO, Methanol
form Solid
pka14.55±0.10(Predicted)
color Off-White
InChIInChI=1S/C11H17NO/c1-11(2,9-13)12-8-10-6-4-3-5-7-10/h3-7,12-13H,8-9H2,1-2H3
InChIKeyJIDHEIXSIHNMCG-UHFFFAOYSA-N
SMILESC(O)C(C)(NCC1=CC=CC=C1)C
CAS DataBase Reference10250-27-8
Safety Information
MSDS Information
2-Benzylamino-2-methyl-1-propanol Usage And Synthesis
Uses2-Benzylamino-2-methyl-1-propanol, as a basic skeleton, is commonly used as an organic ligand in the structural modification and synthesis of oxazoline ligands. These ligands have wide applications in coordination chemistry and organometallic chemistry, playing a particularly important role in catalytic reactions. As a fundamental skeleton in organic synthesis, this molecule is frequently used in basic organic chemistry research to explore new reaction pathways, catalyst design, and synthetic methods for novel organic ligands.
Chemical PropertiesYellow-Orange Solid
Synthesis Reference(s)Tetrahedron, 44, p. 6801, 1988 DOI: 10.1016/S0040-4020(01)86206-2
SynthesisTo a solution of 2-amino-2-methylpropan-1-ol (1 g, 11.22 mmol) and benzaldehyde (1.310 g, 12.34 mmol) in DCE (15 mL) at RT was added portionwise sodium triacetoxyborohydride (6.66 g, 31.4 mmol), and the mixture was stirred for 3 h. The mixture was diluted with EtOAc and washed with saturated aqueous NaHCO3. The organic layer was dried over MgSO4, filtered, and concentrated. The crude product 2-Benzylamino-2-methyl-1-propanol (1.247 g, 6.96 mmol, 62 % yield) was used without further purification. LCMS (m/z): 180.0 (M+H+).synthesis of 2-Benzylamino-2-methyl-1-propanol
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