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

(1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL Structure
CAS No.
57794-08-8
Chemical Name:
(1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL
Synonyms
(1S,2S)-cyclohexane-1,2-diol;(S,S)-(+)-1,2-CYCLOHEXANEDIOL;1,2-Cyclohexanediol, (1S,2S)-;(1S,2S)-1α,2β-Cyclohexanediol;(1S)-TRANS-1,2-CYCLOHEXANEDIOL;[1S,2S,(+)]-1,2-Cyclohexanediol;(1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL;(1S,2S)-trans-1,2-Cyclohexanediol,98%;(1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL 98%;(1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL, 99% ( 99% EE/GLC)
CBNumber:
CB8265320
Molecular Formula:
C6H12O2
Molecular Weight:
116.16
MOL File:
57794-08-8.mol
MSDS File:
SDS
Modify Date:
2022/12/21 16:56:50

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

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS05,GHS07
Signal word  Danger
Hazard statements  H318-H335
Precautionary statements  P261-P280-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37-41
Safety Statements  26-39
WGK Germany  3
HS Code  29061990

(1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 421804 (1S,2S)-trans-1,2-Cyclohexanediol 99% 57794-08-8 250MG ₹6657.38 2022-06-14 Buy
Sigma-Aldrich(India) 421804 (1S,2S)-trans-1,2-Cyclohexanediol 99% 57794-08-8 1G ₹23566.03 2022-06-14 Buy
Product number Packaging Price Buy
421804 250MG ₹6657.38 Buy
421804 1G ₹23566.03 Buy

(1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL Chemical Properties,Uses,Production

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.]

(1S,2S)-TRANS-1,2-CYCLOHEXANEDIOL Preparation Products And Raw materials

Raw materials

Preparation Products

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

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(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 (1S,2S)-cyclohexane-1,2-diol 1,2-Cyclohexanediol, (1S,2S)- 57794-08-8 Organic Building Blocks Polyols Asymmetric Synthesis Chiral Building Blocks