trans-Cyclohexane-1,2-diol structure
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Common Name | trans-Cyclohexane-1,2-diol | ||
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CAS Number | 1460-57-7 | Molecular Weight | 116.158 | |
Density | 1.2±0.1 g/cm3 | Boiling Point | 236.7±8.0 °C at 760 mmHg | |
Molecular Formula | C6H12O2 | Melting Point | 101-104 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 114.3±13.0 °C |
Name | trans-cyclohexane-1,2-diol |
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Synonym | More Synonyms |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 236.7±8.0 °C at 760 mmHg |
Melting Point | 101-104 °C(lit.) |
Molecular Formula | C6H12O2 |
Molecular Weight | 116.158 |
Flash Point | 114.3±13.0 °C |
Exact Mass | 116.083733 |
PSA | 40.46000 |
LogP | 0.15 |
Vapour Pressure | 0.0±1.0 mmHg at 25°C |
Index of Refraction | 1.527 |
Storage condition | -20°C Freezer |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | F: Flammable; |
Safety Phrases | S23-S24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2906199090 |
Precursor 9 | |
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DownStream 10 | |
HS Code | 2906199090 |
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Summary | 2906199090. cyclanic, cyclenic or cyclotherpenic alcohols. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0% |
Heterogeneity and Bipotency of Astroglial-Like Cerebellar Progenitors along the Interneuron and Glial Lineages.
J. Neurosci. 35 , 7388-402, (2015) Cerebellar GABAergic interneurons in mouse comprise multiple subsets of morphologically and neurochemically distinct phenotypes located at strategic nodes of cerebellar local circuits. These cells are... |
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Effect of ethanol on the urinary excretion of cyclohexanol and cyclohexanediols, biomarkers of the exposure to cyclohexanone, cyclohexane and cyclohexanol in humans.
Scand. J. Work. Environ. Health 25(3) , 233-7, (1999) This study explored the acute effect of ethanol (EtOH) on the urinary excretion of cyclohexanol (CH-ol), 1,2- and 1,4-cyclohexanediol (CH-diol), biomarkers of exposure to important solvents, and chemi... |
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Tin(II) chloride catalyzed reactions of diazodiphenylmethane with vicinal diols in an aprotic solvent. The reactions with cis- and trans-1,2-cyclohexanediols and 1,2-propanediol.
Carbohydr. Res. 338(9) , 963-8, (2003) The paper reports the tin(II) chloride catalyzed reactions of diazodiphenylmethane with the cis- and trans-1,2-cyclohexanediols and R,S-1,2-propanediol in 1,2-dimethoxyethane and the identification of... |
racemic trans-1,2-cyclohexanediol |
Cyclohexanediole |
(1R,2R)-1,2-Cyclohexanediol |
Hexahydrocatechol |
(RS,RS)-1,2-trans-cyclohexanediol |
trans-Cyclohexane-1,2-diol |
(1R,2R)-Cyclohexane-1,2-diol |
TRANS-1,2-CYCLOHEX AND IOL |
L6TJ AQ BQ &&trans |
(±)-trans-1,2-Cyclohexanediol |
TRANS-1,2-CYCLOHEXANEDIOL |
(+/-)-trans-1,2-cyclohexanediol |
ca. |
1,2-trans-Cyclohexanediol |
1,2-Cyclohexanediol, (1R,2R)- |
EINECS 215-956-6 |
trans-(1RS,2RS)-cyclohexane-1,2-diol |
MFCD00063611 |
trans-1,2-Dihydroxycyclohexane |