Cyclopropane-1,1-dicarboxylic acid - CAS 598-10-7
Catalog: |
BB030512 |
Product Name: |
Cyclopropane-1,1-dicarboxylic acid |
CAS: |
598-10-7 |
Synonyms: |
cyclopropane-1,1-dicarboxylic acid |
IUPAC Name: | cyclopropane-1,1-dicarboxylic acid |
Description: | Cyclopropane-1,1-dicarboxylic acid (CAS# 598-10-7) is an inhibitor of 1-aminocyclopropane-1-carboxylic Acid oxidase in Lycopersicum esculentum (Tomato plant). It can also be used as a building block for the synthesis of a series of cyclopropanecarboxamides, having antifungal activity. |
Molecular Weight: | 130.10 |
Molecular Formula: | C5H6O4 |
Canonical SMILES: | C1CC1(C(=O)O)C(=O)O |
InChI: | InChI=1S/C5H6O4/c6-3(7)5(1-2-5)4(8)9/h1-2H2,(H,6,7)(H,8,9) |
InChI Key: | FDKLLWKMYAMLIF-UHFFFAOYSA-N |
Boiling Point: | 371.3 °C at 760 mmHg |
Melting Point: | 134-138 °C |
Purity: | 95 % |
Density: | 1.708 g/cm3 |
Appearance: | White crystalline powder. |
Storage: | Store in a cool, dry place. Store in a tightly closed container. Corrosives area. |
MDL: | MFCD00013727 |
LogP: | -0.06420 |
Refractive Index: | 1.5800 (estimate) |
GHS Hazard Statement: | H314 (97.92%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation] |
Precautionary Statement: | P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P405, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
CN-113429954-A | Oil-displacing surfactant system, and preparation method and application thereof | 20210730 |
CN-112852471-A | Method for extracting asphalt in oil sand by aid of eutectic solvent | 20210120 |
CN-112458633-A | Double-component self-crimping high-fluffiness fiber spun-bonded non-woven fabric and preparation method thereof | 20201207 |
CN-111925262-A | Preparation method of multi-component low-eutectic liquid based on metal chloride | 20200819 |
CN-111925262-B | Preparation method of multi-component low-eutectic liquid based on metal chloride | 20200819 |
PMID | Publication Date | Title | Journal |
22812906 | 20120813 | Metal-chelating polymers by anionic ring-opening polymerization and their use in quantitative mass cytometry | Biomacromolecules |
22747000 | 20120731 | Self-assembly of amphiphilic liquid crystal polymers obtained from a cyclopropane-1,1-dicarboxylate bearing a cholesteryl mesogen | Langmuir : the ACS journal of surfaces and colloids |
21696643 | 20110623 | Protocol: An updated integrated methodology for analysis of metabolites and enzyme activities of ethylene biosynthesis | Plant methods |
20944243 | 20101001 | Binding of flexible and constrained ligands to the Grb2 SH2 domain: structural effects of ligand preorganization | Acta crystallographica. Section D, Biological crystallography |
19894700 | 20091204 | trans-Directing ability of the amide group: enabling the enantiocontrol in the synthesis of 1,1-dicarboxy cyclopropanes. Reaction development, scope, and synthetic applications | The Journal of organic chemistry |
Complexity: | 152 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 130.02660867 |
Formal Charge: | 0 |
Heavy Atom Count: | 9 |
Hydrogen Bond Acceptor Count: | 4 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 130.02660867 |
Rotatable Bond Count: | 2 |
Topological Polar Surface Area: | 74.6 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | -0.2 |
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Carbonyl Compounds
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS