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1,1-Cyclopropanedicarboxylic acid

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Products Intro: Product Name:cyclopropane-1,1-dicarboxylic acid
CAS:598-10-7
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Products Intro: Product Name:1,1-Cyclopropanedicarboxylic acid
CAS:598-10-7
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Products Intro: Product Name:1,1-Cyclopropanedicarboxylic acid
CAS:598-10-7
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Products Intro: Product Name:1,1-Cyclopropanedicarboxylic acid
CAS:598-10-7
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1,1-Cyclopropanedicarboxylic acid manufacturers

1,1-Cyclopropanedicarboxylic acid Basic information
Product Name:1,1-Cyclopropanedicarboxylic acid
Synonyms:RARECHEM AL BO 0836;Cycloprpopane-1,1-Dicarboxylic;Cyclopropane-1,1-dicarboxylic acid 97%;1,1-cyclopropanedicarboxylate;1,1-CYCLOPROPANEDICARBOXYLIC ACID;CYCLOPROPANE-1,1-DICARBOXYLIC ACID;1-Carboxycyclopropanecarboxylic acid;1,1-Cyclopropanedicarboxylic acid,98%
CAS:598-10-7
MF:C5H6O4
MW:130.1
EINECS:209-917-2
Product Categories:Building Blocks;C1 to C5;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks;Carboxylic Acids;Organic acids;Cyclopropanes;Simple 3-Membered Ring Compounds;Carboxylic Acids;Ring Systems;C1 to C5;Carbonyl Compounds
Mol File:598-10-7.mol
1,1-Cyclopropanedicarboxylic acid Structure
1,1-Cyclopropanedicarboxylic acid Chemical Properties
Melting point 134-136 °C(lit.)
Boiling point 200.75°C (rough estimate)
density 1.3985 (rough estimate)
refractive index 1.5800 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility methanol: soluble1g/10 mL, clear, colorless
form powder to crystal
pka1.82(at 25℃)
color White to Almost white
Water Solubility Soluble
BRN 1864823
InChIInChI=1S/C5H6O4/c6-3(7)5(1-2-5)4(8)9/h1-2H2,(H,6,7)(H,8,9)
InChIKeyFDKLLWKMYAMLIF-UHFFFAOYSA-N
SMILESC1(C(O)=O)(C(O)=O)CC1
CAS DataBase Reference598-10-7(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,C
Risk Statements 36/37/38-34
Safety Statements 26-36-45-36/37/39
RIDADR UN 3261 8/PG 2
WGK Germany 3
Hazard Note Irritant
HazardClass 8
PackingGroup III
HS Code 29172090
Storage Class8A - Combustible corrosive hazardous materials
Hazard ClassificationsSkin Corr. 1B
MSDS Information
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1,1-Cyclopropanedicarboxylic acid English
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1,1-Cyclopropanedicarboxylic acid Usage And Synthesis
Chemical Propertieswhite to almost white crystalline powder
Uses1,1-Cyclopropanedicarboxylic acid is used to prepare spiro-cyclopropyl metallocycles.1
Uses1,1-Cyclopropanedicarboxylic acid, is used as an inhibitor of 1-aminocyclopropane-1-carboxylic acid oxidase, was quantitated in Lycopersicum esculentum by HPLC-electrospray tandem mass spectrometry. Crystal and molecular structure of cyclopropane-1,1-dicarboxylic acid has been reported. Cyclopropane-1,1-dicarboxylic acid was used in the preparation of new heterocyclic derivatives of cyclopropane dicarboxylic acid containing thiadiazole and 1,2,4-triazole moieties. It was also used to prepare spiro-cyclopropyl metallocycles. It can also be used as a building block for the synthesis of a series of cyclopropanecarboxamides, having antifungal activity.
General DescriptionCyclopropane-1,1-dicarboxylic acid is a dicarboxylic acid. Cyclopropane-1,1-dicarboxylic acid, an inhibitor of 1-aminocyclopropane-1-carboxylic acid oxidase, was quantitated in Lycopersicum esculentum by HPLC-electrospray tandem mass spectrometry. Crystal and molecular structure of cyclopropane-1,1-dicarboxylic acid has been reported.
Synthesis
1,2-Dibromoethane

106-93-4

Diethyl malonate

105-53-3

1,1-Cyclopropanedicarboxylic acid

598-10-7

GENERAL STEPS: 15 g of diethyl malonate was dissolved in 187 ml of aqueous solution containing 50 μl NaOH at room temperature. Subsequently 21.3 g (93.8 mmol) of benzyltriethylammonium chloride was added and the resulting mixture was stirred for 10 minutes. To the reaction solution was added 12.3 g (65.47 mmol) of 1,2-dibromoethane and the reaction mixture continued to be stirred at room temperature for more than 18 hours. Upon completion of the reaction, the reaction mixture was neutralized by adding acid solution dropwise. The reaction mixture was washed with aqueous sulfuric acid solution and subsequently extracted with ethyl acetate. The organic phases were combined and the solvent was removed by distillation under reduced pressure to afford 6.2 g of a white solid product, 1,1-cyclopropanedicarboxylic acid, in 76.1% yield.

Purification MethodsRecrystallise the di-acid from CHCl3, EtOAc or *C6H6/Et2O/pet ether. It forms a monohydrate. [Nicolet & Satler J Am Chem Soc 49 2070 1927, Beilstein 9 II 512, 9 III 3795.]
References[1] Organic Letters, 2015, vol. 17, # 11, p. 2618 - 2621
[2] Bioorganic and Medicinal Chemistry, 2016, vol. 24, # 16, p. 3353 - 3358
[3] Bioorganic and Medicinal Chemistry, 2017, vol. 25, # 24, p. 6674 - 6679
[4] Mendeleev Communications, 2014, vol. 24, # 6, p. 345 - 345
[5] Patent: WO2005/79812, 2005, A1. Location in patent: Page/Page column 51
Tag:1,1-Cyclopropanedicarboxylic acid(598-10-7) Related Product Information
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