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ChemicalBook >  Product Catalog >  Organic Chemistry >  Alcohols,Phenols,Phenol alcohols >  (1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL

(1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL

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(1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL Basic information

Product Name:
(1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL
Synonyms:
  • (1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL
  • (1S)-TRANS-1,2-CYCLOHEXANEDIOL
  • (1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL, 99% ( 99% EE/GLC)
  • (1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL 98%
  • (1S,2S)-1α,2β-Cyclohexanediol
  • [1S,2S,(+)]-1,2-Cyclohexanediol
  • (1S,2S)-trans-1,2-Cyclohexanediol,98%
  • (S,S)-(+)-1,2-CYCLOHEXANEDIOL
CAS:
57794-08-8
MF:
C6H12O2
MW:
116.16
Mol File:
57794-08-8.mol
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(1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL Chemical Properties

Melting point:
107-109 °C(lit.)
Boiling point:
177.22°C (rough estimate)
Density 
0.9958 (rough estimate)
refractive index 
1.4270 (estimate)
Flash point:
134 °C
pka
14.49±0.40(Predicted)
optical activity
[α]20/D +39°, c = 1.6 in H2O
BRN 
1901343
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37-41
Safety Statements 
26-39
WGK Germany 
3
HS Code 
29061990

MSDS

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(1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL Usage And Synthesis

Chemical Properties

white to off-white crystals

Uses

(1S,2S)-trans-1,2-Cyclohexanediol may be used in the preparation of (1S,2S)-1,2-cyclohexanediyl bis(4-vinylbenzoate) by reacting with 4-vinylbenzoyl chloride. It may also be used as a chiral ligand for the preparation of non-racemic hydroxy phosphonates via titanium alkoxide-catalyzed addition of dimethyl phosphite to the corresponding aldehydes.

Purification Methods

The enantiomers have been recrystallised from *C6H6 or EtOAc. The (±) diol has been resolved via the distrychnine salt of the hemisulfate [Hayward et al. J Chem Soc Perkin Trans 1 2413 1976], or the 1-menthoxy acetates. {l-trans-diastereoisomer has m 64o, []D -91.7o (c 1.4 EtOH) from pet ether or aqueous EtOH and yields the (-)-trans-diol } and {d-trans-diastereoisomer has m 126-127o, []D -32.7o (c 0.8 EtOH) from pet ether or aqueous EtOH and yields the (+)-trans diol}. The bis-4-nitrobenzoate has m 126.5o []D (-) and (+) 25.5o (c 1.1 CHCl3), and the bis-3,5-dinitrobenzoate has m 160o []D ± 83.0o (c 1.8 CHCl3) [Wilson & Read J Chem Soc 1269 1935]. [Beilstein 6 III 4060.]

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