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

(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
EINECS:
Product Categories:
Mol File:57794-08-8.mol
(1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL Structure
(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)
Fp 134 °C
pka14.49±0.40(Predicted)
optical activity[α]20/D +39°, c = 1.6 in H2O
BRN 1901343
Safety Information
Hazard Codes Xi
Risk Statements 36/37-41
Safety Statements 26-39
WGK Germany 3
HS Code 29061990
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
(1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL Usage And Synthesis
Chemical Propertieswhite 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 MethodsThe 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.]
(1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL Preparation Products And Raw materials
L-QUEBRACHITOL Neomycin sulfate RIBOSTAMYCIN SULFATE SALT D-INS(1,4,5)P3, 3LI BUTIROSIN DISULFATE D-MYO-INOSITOL 1,4,5-TRISPHOSPHATE HEXASODIUM SALT FORSKOLIN, 7-DEACETYL-7-O-HEMISUCCINYL- HEXA(2-CYANOETHOXY) CYCLOHEXANE EPI-INOSITOL Inositol nicotinate MYO-INOSITOL 2-MONOPHOSPHATE DI(CYCLOHEXYLAMMONIUM) SALT Geneticin VERATRINE (-)-4,5-O-CYCLOHEXYLIDENEQUINIC ACID LACTONE MYO-INOSITOL HEXASULFATE HEXAPOTASSIUM SALT 1L-EPI-2-INOSOSE Spectinomycin INS(1,3,4,5)P4

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