Basic information Safety Supplier Related

2-Cyclohexylmandelic acid

Basic information Safety Supplier Related

2-Cyclohexylmandelic acid Basic information

Product Name:
2-Cyclohexylmandelic acid
Synonyms:
  • acidephenylcyclohexylhydroxyacetique
  • alpha-cyclohexyl-alpha-hydroxy-benzeneaceticaci
  • alpha-cyclohexyl-alpha-hydroxybenzeneaceticacid
  • alpha-phenyl-cyclohexaneglycolicaci
  • alpha-phenylcyclohexaneglycolicacid
  • ALPHA CYCLOHEXYL MANDELIC ACID ( CAS: )
  • Benzeneacetic acid,α-cyclohexyl-α-hydroxy-
  • α-Cyclohexylmandelic acid
CAS:
4335-77-7
MF:
C14H18O3
MW:
234.29
EINECS:
224-380-4
Product Categories:
  • Pharmaceutical Intermediates
  • Aromatics
Mol File:
4335-77-7.mol
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2-Cyclohexylmandelic acid Chemical Properties

Melting point:
163 °C
Boiling point:
135℃/3mm
Density 
1.206±0.06 g/cm3(Predicted)
RTECS 
GV2770000
storage temp. 
-20°C Freezer
solubility 
Chloroform (Slightly), Methanol (Sparingly)
form 
Solid
pka
3.49±0.25(Predicted)
color 
White to pale brown
CAS DataBase Reference
4335-77-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
37/38-41
Safety Statements 
26-39
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29181990
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2-Cyclohexylmandelic acid Usage And Synthesis

Description

This indole alkaloid occurs in the leaves of Lespedeza bicolor var. japonica and, when pure, is a colourless oil. Its MeOH solution, the ultraviolet spectrum exhibits absorption maxima at 223.4, 279 and 291 mJi. The crystalline hydrochloride has m.p. 163-4°C (dec.); the picrate forms long, yellow needles from MeOH, m.p. 160-2°C (dec.) and the styphnate, also yellow needles, has m.p. 170°C (dec.). The structure has been established as 3-(dimethylaminoethyl)-1-methoxyindole.

Chemical Properties

White Solid

Uses

An intermediate in the synthesis of oxybutynin (O868525). Oxybutynin USP Related Compound A.

Uses

intermediate for Oxybutynin HCl, Oxyphenonium Bromide

Definition

ChEBI: Alpha-Cyclohexylmandelic acid is a member of benzenes.

References

Morimoto, Oshio., Annalen, 682, 212 (1965)

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