Cyclopentane-1,2,3,4-tetracarboxylic acid

Base Information

• Chemical Name: Cyclopentane-1,2,3,4-tetracarboxylic acid
• CAS No.: 3724-52-5
• Molecular Formula: C9H10O8
• Molecular Weight: 246.174
• Hs Code.: 2917209090
• European Community (EC) Number: 223-256-7,223-074-8
• DSSTox Substance ID: DTXSID30958404
• Nikkaji Number: J205.635F
• Mol file: 3724-52-5.mol

Synonyms:Cyclopentane-1,2,3,4-tetracarboxylic acid;3724-52-5;1,2,3,4-Cyclopentanetetracarboxylic acid;3786-91-2;1,2,3,4-Cyclopentanetetracarboxylicacid;1,2,3,4-Tetracarboxycyclopentane;EINECS 223-074-8;EINECS 223-256-7;r-1,c-2,c-3,c-4-Cyclopentanetetracarboxylic acid;AI3-50868;C9-H10-O8;MFCD00001377;Oprea1_132715;SCHEMBL22039;C9H10O8;DTXSID30958404;BBL012265;NSC 73712;STK803135;1,2,3,4-cyclo-pentanetetracarboxylic;AKOS003368776;AKOS016844207;LS-58045;VS-03254;1,2,3,4-cyclopentane tetracarboxylic acid;FT-0623866;FT-0709796;D89313;1,2,3,4-Cyclopentanetetracarboxylic acid, (1alpha,2alpha,3alpha,4alpha)-

Chemical Property of Cyclopentane-1,2,3,4-tetracarboxylic acid

Chemical Property:

• Melting Point: approximate 179℃ (dec.)
• Boiling Point: 495.6 °C at 760 mmHg
• PKA: 3.44±0.70(Predicted)
• Flash Point: 267.6 °C
• PSA: 149.20000
• Density: 1.787 g/cm³
• LogP: -0.80670
• Solubility.: almost transparency in Methanol
• XLogP3: -1.5
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 4
• Exact Mass: 246.03756727
• Heavy Atom Count: 17
• Complexity: 351

Purity/Quality:

99.0% ^*data from raw suppliers

Cyclopentane-1,2,3,4-tetracarboxylicAcid ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C(C(C(C1C(=O)O)C(=O)O)C(=O)O)C(=O)O

Technology Process of Cyclopentane-1,2,3,4-tetracarboxylic acid

There total 21 articles about Cyclopentane-1,2,3,4-tetracarboxylic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 87.04%

C9H10O6 → cyclopentane-1,2,3,4-tetracarboxylic acid (3724-52-5)

Guidance literature:

With dihydrogen peroxide; at 80 ℃; Temperature;

Reference yield: 81.0%

all-cis-tetra(n-propyl) cyclopentanetetracarboxylate (16550-49-5) → all-trans-cyclopentanetetracarboxylic acid (3724-52-5,3786-91-2,69432-65-1,82395-69-5,150617-78-0)

Guidance literature:

With sodium hydroxide; In methanol;

Reference yield: 59.9%

→ cyclopentane-1,2,3,4-tetracarboxylic acid (3724-52-5)

Guidance literature:

With formic acid; p-toluenesulfonic acid monohydrate; In acetonitrile;

upstream raw materials:

5-norbornene-2,3-dicarboxylic anhydride

norbornene-5,6-dicarboxylic acid

hydrogenchloride

cis,cis,cis,cis-1,2,3,4-cyclopentanetetracarboxylic acid

Downstream raw materials:

1,2,3,4-cyclopentanetetracarboxylic acid dianhydride

all-trans-cyclopentanetetracarboxylic acid

cis,cis,cis,cis-cyclopentane-1,2,3,4-tetracarboxylic acid

(+/-)-cyclopentane-1r,2c,3t,4c-tetracarboxylic acid-1,2;3,4-dianhydride

Refernces

• 1、 -. "CAGE-SHAPED CYCLOPENTANOIC DIANHYDRIDE, METHOD FOR PRODUCTION THEREOF, AND POLYIMIDE". Page/Page column. . Retrieved 2014/05/07.
• 2、 Somekawa, Kenichi,Nomura, Masafumi,Aoki, Shoichi,Noma, Shinji,Shimo, Tetsuro. "SYNTHESIS OF TETRASUBSTITUTED CYCLOPENTANES". . p. 449 - 456. Retrieved 2007/10/02.