Identification | Back Directory | [Name]
(+/-)-TRANS-1,2-CYCLOHEXANEDICARBOXYLIC ANHYDRIDE | [CAS]
14166-21-3 | [Synonyms]
Einecs 238-009-9 TRANS-HEXAHYDROPHTHALIC ANHYDRIDE trans-Hexahydroisobenzofuran-1,3-dione 1,3-Isobenzofurandione, hexahydro-, trans- TRANS-1,2-CYCLOHEXANEDICARBOXYLIC ANHYDRIDE trans-cyclohexane-1,2-dicarboxylic anhydride trans-1,2-Cyclohexanedicarboxylic anhydride 97% (+/-)-TRANS-1,2-CYCLOHEXANEDICARBOXYLIC ANHYDRIDE 1,3-Isobenzofurandione,hexahydro-, (3aR,7aR)-rel- cis-1.2-Cyclohexane dicarboxylic anhydride 1g [14166-21-3] trans-1,2-Cyclohexanedicarboxylic anhydride,trans-Hexahydrophthalic anhydride | [EINECS(EC#)]
238-009-9 | [Molecular Formula]
C8H10O3 | [MDL Number]
MFCD00064345 | [MOL File]
14166-21-3.mol | [Molecular Weight]
154.16 |
Chemical Properties | Back Directory | [Melting point ]
145-147 °C(lit.)
| [Boiling point ]
283.4±0.0 °C(Predicted) | [density ]
1.235±0.06 g/cm3(Predicted) | [storage temp. ]
2-8°C | [solubility ]
Acetone (Sparingly), Chloroform (Slightly), DMSO (Slightly) | [form ]
Solid | [color ]
White to Pale Beige | [Stability:]
Moisture Sensitive | [CAS DataBase Reference]
14166-21-3 |
Hazard Information | Back Directory | [Uses]
Trans-1,2-cyclohexanedicarboxylic anhydride can be used as a reagent to prepare hepatitis C virus (HCV) and granzyme B (indoline derivatives) inhibitors. It has also been employed in studies relating to the development of protein kinase C inhibitors. | [Purification Methods]
Crystallise the anhydride from *C6H6/Et2O. It has been obtained by heating the cis-acid or anhydride with HCl at 180o for 3hours. It can be obtained from the acid by heating in Ac2O. It sublimes at 125-135o/0.02mm. [Kohler & Jansen J Am Chem Soc 60 2145 1938, Fichter & Simon Helv Chim Acta 17 1218 1934, Beilstein 9 IV 2802.] |
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