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(S)-tert-Leucinol

Names

[ CAS No. ]:
112245-13-3

[ Name ]:
(S)-tert-Leucinol

[Synonym ]:
(R)-(−)-tert-Leucinol
(2R)-2-amino-3,3-dimethylbutan-1-ol
MFCD00192250
(R)-tert-Leucinol
(R)-2-Amino-3,3-dimethylbutan-1-ol
(2S)-2-Amino-3,3-dimethyl-1-butanol
L-t-butyl leucinol
1-Butanol, 2-amino-3,3-dimethyl-, (2S)-
H-TLE-OL
L-T-LEUCINOL
L-Tert-Leucinol
(2S)-2-Amino-3,3-dimethylbutan-1-ol
(S)-2-Amino-3,3-dimethylbutanol
L-T-BUTYLGLYCINOL
(S)-2-Amino-3,3-dimethyl butanol

Chemical & Physical Properties

[ Density]:
0.9

[ Boiling Point ]:
198.5±13.0 °C at 760 mmHg

[ Melting Point ]:
30-34ºC(lit.)

[ Molecular Formula ]:
C6H15NO

[ Molecular Weight ]:
117.189

[ Flash Point ]:
90 ºC

[ Exact Mass ]:
117.115364

[ PSA ]:
46.25000

[ LogP ]:
0.27

[ Vapour Pressure ]:
0.1±0.8 mmHg at 25°C

[ Index of Refraction ]:
1.452

[ Storage condition ]:
2-8°C

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S37/39

[ RIDADR ]:
1325.0

[ WGK Germany ]:
3

[ Hazard Class ]:
4.1

[ HS Code ]:
2922199090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2922199090

[ Summary ]:
2922199090. other amino-alcohols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Synthesis and Properties of a Novel Pyridineoxazoline Containing Optically Active Helical Polymer as a Catalyst Ligand for Asymmetric Diels-Alder Reaction.

Chirality 27 , 523-31, (2015)

A novel pyridineoxazoline (PyOx) containing helical polymer, poly{(-)-(S)-4-tert-butyl-2-[5-(4-tert-butylphenyl)-3-vinylpyridin-2-yl]-oxazoline} (PA), was designed and synthesized to approach the effe...

SimplePHOX, a readily available chiral ligand system for iridium-catalyzed asymmetric hydrogenation.

Org. Lett. 6 , 2023-2026, (2004)

[reaction: see text] New Ir-SimplePHOX complexes Ir-6-Ir-9 catalyze the quantitative, highly enantioselective hydrogenation of a range of unfunctionalized and functionalized olefins. Synthesis, cataly...

Tetrahedron Lett. 45 , 5649, (2004)


More Articles


Related Compounds

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