(S)-1-(2-aminophenyl)ethan-1-ol

Synonym
Product Category
Product Code
CAS Number
MDL Number
Pubchem CID
Reaxys RN
(S)-1-(2'-aminophenyl)ethanol
Non-Fluorochemicals
KUMI0F72
3205-21-8

 
6475347
image-155171-Trimethyl(trifluoromethyl)silane_reagent.png
Chemical Name
Molecular Formula
Molecular Weight
Assay
Appearance
Boilng Point
Packaging
Storage
(S)-1-(2-aminophenyl)ethan-1-ol
C8H11NO
137.18
≥98%
Pale yellow to Brown Soid
54-59°C
50g,100g,250g,500g and 1kg
Store at room temperature
(S)-1-(2-aminophenyl)ethan-1-ol is a key intermediate for the synthesis of chiral compounds, e.g. Chiral organoselenanes and organotelluranes.
A Molybdenum-Catalyzed Oxidative System Forming Oxazines (Hetero-Diels−Alder Adducts) from Primary Aromatic Amines, Hydrogen Peroxide, and Conjugated Dienes. [1]
An enantiopure galactose oxidase model: synthesis of chiral amino alcohols through oxidative kinetic resolution catalyzed by a chiral copper complex. [2]
Asymmetric hydrogenation of aromatic ketones by chiral (1S,2S)-DPEN-Ru(II)Cl2(TPP)2 encapsulated in SBA-16. [3]
Enzymatic kinetic resolution of tert-butyl 2-(1-Hydroxyethyl) phenylcarbamate, a key intermediate to chiral organoselenanes and organotelluranes. [4]
References:
[1] E.R.Moller, et al, J. Org. Chem., 1996, 61(17), pp 5770-5778.
[2] S.Mannam, et al, Tetrahedron:Asymmetry, 2009, 20(4), pp 497-502.
[3] J.Liu, et al, Cataly. Commun., 2010, 11(5), pp 373-377.
[4] L.Piovan, et al, Molecules, 2011, 16(9), pp 8098-9109.
Signal Word
Hazard Statements
Precautionary Statements
HS Code
RIDADR
Legal Information
Warning
H315,H319,H335
P261,P305+P351+P338
2922190090
NONH for all modes of transport.

1. Product Specification
2. Safety Data Sheet
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