Mucochloric anhydride

Base Information

• Chemical Name: Mucochloric anhydride
• CAS No.: 4412-09-3
• Molecular Formula: C₈H₂Cl₄O₅
• Molecular Weight: 319.913
• Hs Code.: 2932209090
• NSC Number: 14027
• DSSTox Substance ID: DTXSID8041533
• Nikkaji Number: J8.719J
• Mol file: 4412-09-3.mol

Synonyms:Mucochloric anhydride;Muchloric anhydride;Caswell No. 584A;4412-09-3;Bis(3,4-dichlorofuranon-5-yl-2) ether;Bis(3,4-dichloro-2(5)-furanonyl) ether;NSC 14027;EPA Pesticide Chemical Code 584200;GC-2466;AI3-18618;5,5'-Oxybis[3,4-dichloro-2(5H)-furanone];2(5H)-FURANONE, 5,5'-OXYBIS(3,4-DICHLORO-;Crotonic acid, 4,4'-oxybis(2,3-dichloro-4-hydroxy-, di-gamma-lactone;5,5'-Oxybis(3,4-dichloro-2(5H)-furanone);UNII-QC354E4T6V;SCHEMBL414388;QC354E4T6V;DTXSID8041533;NSC14027;NSC-14027;GC 2466;LS-70514;2(5H)-Furanone,5'-oxybis[3,4-dichloro-;WLN: T5OV EHJ CG DG EO- ET5OV EHJ CG DG;bis(2-oxo-3,4-dichloro-2,5-dihydrofuran-5-yl)ether;Crotonic acid,4'-oxybis(2,3-dichloro-4-hydroxy-, di-.gamma.-lactone

Chemical Property of Mucochloric anhydride

Chemical Property:

• Melting Point: 141-143°; mp 180°
• Refractive Index: 1.5282 (estimate)
• Boiling Point: 498.4°Cat760mmHg
• Flash Point: 225.4°C
• PSA: 61.83000
• Density: 1.88g/cm³
• LogP: 2.14720
• XLogP3: 2.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 2
• Exact Mass: 319.862684
• Heavy Atom Count: 17
• Complexity: 427

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1(C(=C(C(=O)O1)Cl)Cl)OC2C(=C(C(=O)O2)Cl)Cl
• Uses: Fungicide. Ref: Gilbert, US 2861919 (1958 to Allied Chem.).

Technology Process of Mucochloric anhydride

There total 3 articles about Mucochloric anhydride 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:

→ bis-(3,4-dichloro-5-oxo-2,5-dihydro-[2]furyl)-ether (4412-09-3)

Guidance literature:

With 1,4-dioxane; benzenesulfonic acid; benzene; optically inactive stereoisomer(ic) of mp: 180 degree;

DOI:10.1021/ja01162a056

Reference yield:

→ bis-(3,4-dichloro-5-oxo-2,5-dihydro-[2]furyl)-ether (4412-09-3)

Guidance literature:

With 1,4-dioxane; benzenesulfonic acid; benzene; optically inactive stereoisomer(ic) of mp: 143 degree;

DOI:10.1021/ja01162a056

Reference yield:

→ C8H2Cl4O5 (4412-09-3,40636-40-6,40636-41-7)

Guidance literature:

aus I, H2SO4, neben IVb;