(R)-(+)-1-Phenylethanol

(R)-(+)-1-Phenylethanol Basic information

Product Name:	(R)-(+)-1-Phenylethanol
Synonyms:	(R)-(+)-PHENYLETHANOL;(R)-(+)-SEC-PHENETHYL ALCOHOL;(R)-(+)-SEC-PHENYLETHYL ALCOHOL;(R)-(+)-1-METHYLBENZYL ALCOHOL;(R)-(+)-1-PHENYLETHYL ALCOHOL;(R)-(+)-1-PHENYLETHANOL;(R)(+)-ALPHA-PHENETHYL ALCOHOL;(R)-(+)-ALPHA-METHYLBENZYL ALCOHOL
CAS:	1517-69-7
MF:	C8H10O
MW:	122.16
EINECS:	604-814-2
Product Categories:	chiral;Building Blocks for Liquid Crystals;Chiral Building Blocks;Chiral Compounds (Building Blocks for Liquid Crystals);Functional Materials;Simple Alcohols (Chiral);Synthetic Organic Chemistry;Alcohols;Chiral Building Blocks;Organic Building Blocks;Alcohols, Hydroxy Esters and Derivatives;Chiral Compounds
Mol File:	1517-69-7.mol

(R)-(+)-1-Phenylethanol Chemical Properties

Melting point	9-11 °C (lit.)
Boiling point	88-89 °C/10 mmHg (lit.)
alpha	42.5 º (NEAT)
density	1.012 g/mL at 20 °C (lit.)
refractive index	n20/D 1.528
Fp	85 °C
storage temp.	Sealed in dry,Room Temperature
solubility	20g/l
pka	14.43±0.20(Predicted)
form	clear liquid
color	Colorless to Light yellow
PH	7 (H2O)
Odor	at 100.00 %. floral earthy green honeysuckle
Odor Type	floral
optical activity	[α]22/D +44.0°, c = 5%
Water Solubility	20 G/L (20 ºC)
BRN	2039798
Stability:	Stable. Flammable. Incompatible with strong acids, strong oxidizing agents.
InChIKey	WAPNOHKVXSQRPX-SSDOTTSWSA-N
LogP	1.420
CAS DataBase Reference	1517-69-7(CAS DataBase Reference)
NIST Chemistry Reference	Benzenemethanol, «alpha»-methyl-, (R)-(1517-69-7)

Safety Information

MSDS Information

(R)-(+)-1-Phenylethanol Usage And Synthesis

Chemical Properties	Colorless to light yellow liqui
Uses	(R)-(+)-1-Phenylethanol is used in the synthesis of optically active products. It is also useful in the determination of enantiomeric purity and for resolutions of acids.
Definition	ChEBI: (R)-1-phenylethanol is the (R)-enantiomer of 1-phenylethanol. It has a role as an animal metabolite. It is an enantiomer of a (S)-1-phenylethanol.
General Description	(R)-1-Phenylethanol can be prepared from ethylbenzene via enantioselective hydroxylation of ethylbenzene catalyzed by peroxygenase enzyme.

(R)-(+)-1-Phenylethanol Preparation Products And Raw materials

Raw materials	Carbamic acid, [(1R,2S)-2-aminocyclopentyl]-, 1,1-dimethylethyl ester, rel--->Carbamic acid, [(1R,2S)-2-aminocyclopentyl]-, 1,1-dimethylethyl ester (9CI)-->Carbamic acid, [(1S,2R)-2-aminocyclopentyl]-, 1,1-dimethylethyl ester (9CI)
Preparation Products	(S)-(-)-1-PHENYLETHANOL-->(-)-[(S)-1-Bromoethyl]benzene-->AM095

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