Detail of > 1759-71-3
- CAS Number:
- 1759-71-3
- Name:
1,2-Cyclohexanediol,1,2-diacetate, (1R,2R)-rel-
- Superlist Name:
- cis-1,2-Cyclohexanediol diacetate
- Formula:
- C10H16O4
- Molecular Structure:
- Synonyms:
- 1,2-Cyclohexanediol,diacetate, (1R,2R)-rel- (9CI);1,2-Cyclohexanediol, diacetate, trans- (8CI);
- Molecular Weight:
- 200.23
- Density:
- 1.092 g/cm3
- Boiling Point:
- 249.661 °C at 760 mmHg
- Flash Point:
- 115.443 °C
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Reference
- Conformational characteristics of trans-1,2-disubstituted derivatives of cyclohexane with electronegative substituents (based on carbon-13 NMR spectral data)
- Conformational characteristics of trans-1,2-disubstituted derivatives of cyclohexane with electronegative substituents (based on carbon-13 NMR spectral data). Zefirov, N. S.; Samoshin, V. V.; Baranenkov, I. V.; Subbotin, O. A.; Sergeev, N. There are some commonly used reagents like 1759-71-3 in this article. M. (Mosk. Gos. 1759-71-3 which is the cas registry number is also used here. Univ., Moscow, USSR). Zh. Org. Khim., 13(10), 2232-3 (Russian) 1977. CODEN: ZORKAE. DOCUMENT TYPE: Journal CA Section: 22 (Physical Organic Chemistry) The free energy difference between the axial-axial and equatorial-equatorial conformations of I (R = F, MeO, AcO; R1 = OH, AcO, MeO, Cl, Br, I) varied from 0.28 to >1.5 kcal/mol. ..
- Conformational characteristics of trans-1,2-disubstituted derivatives of cyclohexane with electronegative substituents (based on carbon-13 NMR spectral data)
- Conformational characteristics of trans-1,2-disubstituted derivatives of cyclohexane with electronegative substituents (based on carbon-13 NMR spectral data). Zefirov, N. S.; Samoshin, V. V.; Baranenkov, I. V.; Subbotin, O. A.; Sergeev, N. There are some commonly used reagents like 1759-71-3 in this article. M. (Mosk. Gos. 1759-71-3 which is the cas registry number is also used here. Univ., Moscow, USSR). Zh. Org. Khim., 13(10), 2232-3 (Russian) 1977. CODEN: ZORKAE. DOCUMENT TYPE: Journal CA Section: 22 (Physical Organic Chemistry) The free energy difference between the axial-axial and equatorial-equatorial conformations of I (R = F, MeO, AcO; R1 = OH, AcO, MeO, Cl, Br, I) varied from 0.28 to >1.5 kcal/mol. ..
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