Cyclopropane-1,1-dicarboxylic acid
Cyclopropane-1,1-dicarboxylic acid structure
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Common Name | Cyclopropane-1,1-dicarboxylic acid | ||
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| CAS Number | 598-10-7 | Molecular Weight | 130.099 | |
| Density | 1.7±0.1 g/cm3 | Boiling Point | 371.3±25.0 °C at 760 mmHg | |
| Molecular Formula | C5H6O4 | Melting Point | 134-136 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 192.5±19.7 °C | |
| Symbol |
GHS05 |
Signal Word | Danger | |
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The simultaneous determination of 1-aminocyclopropane-1-carboxylic acid and cyclopropane-1,1-dicarboxylic acid in Lycopersicum esculentum by high-performance liquid chromatography--electrospray tandem mass spectrometry.
Phytochem. Anal. 14(6) , 347-51, (2003) Varying concentrations of cyclopropane-1,1-dicarboxylic acid (CDA), an inhibitor of 1-aminocyclopropane-1-carboxylic acid oxidase, added to the solid culture medium of tomato nodal shoot segments resulted in a reduction in the level of endogenous ethylene acc... |
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Synthesis of thiadiazoles and 1,2,4-triazoles derived from cyclopropane dicarboxylic acid.
Molecules 10(9) , 1153-60, (2005) New heterocyclic derivatives of cyclopropane dicarboxylic acid comprising thiadiazole and 1,2,4-triazole moieties are reported. Reaction of 1,1-cyclopropane dicarboxylic acid (1) with thiosemicarbazide and phosphorous oxychloride resulted in 1,1-bis (2-amino-... |
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Expedient synthesis of pyrrolo[1,2-a]indoles: preparation of the core of yuremamine.
Org. Lett. 10(16) , 3497-500, (2008) Pyrrolo[1,2- a]indoles are conveniently prepared from tetrahydro-1,2-oxazines, which in turn are generated through the reaction of nitrones with 1,1-cyclopropanediesters. The synthetic route proves to be highly diastereoselective and provides access to the co... |
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Scandium triflate catalyzed cycloaddition of imines with 1,1-cyclopropanediesters: efficient and diastereoselective synthesis of multi-substituted pyrrolidines.
Org. Biomol. Chem. 4(2) , 299-301, (2006) A tandem ring-opening-cyclization reaction of cyclopropanes with imines in the presence of 5 mol% of scandium triflate was developed for the highly diastereoselective synthesis of multi-substituted pyrrolidines. |
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Prime site binding inhibitors of a serine protease: NS3/4A of hepatitis C virus.
Biochemistry 41(17) , 5483-92, (2002) Serine proteases are the most studied class of proteolytic enzymes and a primary target for drug discovery. Despite the large number of inhibitors developed so far, very few make contact with the prime site of the enzyme, which constitutes an almost untapped ... |
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Studies on structures of some platinum complexes with 1,1-cyclopropanedicarboxylate.
Sci. China,. Ser. B, Chem. Life Sci. Earth Sci. 33(11) , 1297-303, (1990) The crystal structures of [Pt(NH3)2CPrDCA].H2O (I), [Pt(CH3NH2)2CPrDCA] (II), and [Pt(dmbn) CPrDCA].2.5H2O (III) (where CPrDCA is 1,1-cyclopropanedicarboxylate; dmbn is 2,3-dimethyl-2,3-butyldiamine) are determined. Compound I crystallizes in the orthorhombic... |
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Tetrahedron 45 , 1219, (1989)
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The crystal and molecular structure of cyclopropane-1, 1-dicarboxylic acid. Meester MAM, et al.
Acta Crystallogr. B 27(3) , 630-34, (1971)
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