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(S)-(+)-2-Phenylglycinol

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(S)-(+)-2-Phenylglycinol Basic information

Product Name:
(S)-(+)-2-Phenylglycinol
Synonyms:
  • L-(+)-ALPHA-PHENYLGLYCINOL
  • L-(+)-A-PHENYLGLYCINOL
  • L-2-PHENYLGLYCINOL
  • L-beta-Aminophenethyl alcohol
  • H-PHG-OL
  • H-PHENYLGLYCINOL
  • H-L-PHG-OL
  • D-2-PHENYLGLYCINOL
CAS:
20989-17-7
MF:
C8H11NO
MW:
137.18
EINECS:
606-683-7
Product Categories:
  • Amines
  • Aromatics
  • Amino Alcohols (Chiral)
  • Chiral Reagents
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • chiral
  • Chiral Reagent
  • Amino Acids 13C, 2H, 15N
  • Asymmetric Synthesis
  • Chiral Building Blocks
  • Synthetic Organic Chemistry
  • Amino alcohols
  • Amino Acids & Derivatives
  • Pharmaceutical Intermediates
  • Alcohols and Derivatives
  • Phenylglycine [Phg]
Mol File:
20989-17-7.mol
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(S)-(+)-2-Phenylglycinol Chemical Properties

Melting point:
76-79 °C
alpha 
-25.5 º (c=6, MeOH)
Boiling point:
252.03°C (rough estimate)
Density 
1.0630 (rough estimate)
refractive index 
30 ° (C=1, EtOH)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
pka
12.51±0.10(Predicted)
form 
Crystalline Powder
color 
White to pale yellow
optical activity
[α]19/D +33°, c = 0.75 in 1 M HCl
Water Solubility 
Soluble in chloroform, dimethylsulfoxide and methanol. Limited solubility in water.
Sensitive 
Air Sensitive
BRN 
3196190
CAS DataBase Reference
20989-17-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
C,T
Risk Statements 
34-36/37/38-23/24/25
Safety Statements 
22-24/25-45-36/37/39-26-37
WGK Germany 
3
2-10
HS Code 
29052900

MSDS

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(S)-(+)-2-Phenylglycinol Usage And Synthesis

Chemical Properties

white to light yellow crystal powde

Uses

(S)-(+)-2-Phenylglycinol is used in the synthesis of chiral, unsymmetrical bisoxazolines. It is used as a reagent for the resolution of acids via the easily hydrolyzed amides.

Uses

(S)-(+)-2-Phenylglycinol is a chiral arylalkylamine used as organocatalysts. Used in the synthesis and chiral recognition properties of novel fluorescent chemosensors for amino acid.

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