Quinonamid

Base Information

• Chemical Name: Quinonamid
• CAS No.: 27541-88-4
• Molecular Formula: C12H6 Cl3 N O3
• Molecular Weight: 318.544
• Hs Code.: 2924299090
• European Community (EC) Number: 248-516-7
• UNII: 618QV11Q2U
• DSSTox Substance ID: DTXSID2058047
• Nikkaji Number: J9.901E
• Wikidata: Q27155784
• Mol file: 27541-88-4.mol

Synonyms:Quinonamid;27541-88-4;Chinonamid;Alginex;Quinonamid [ISO];HOE 134650H;2-(Dichloroacetylamino)-3-chloronaphthoquinone;1,4-Naphthoquinone, 2-chloro-3-(2,2-dichloroacetamido)-;EINECS 248-516-7;2,2-dichloro-N-(3-chloro-1,4-dioxonaphthalen-2-yl)acetamide;BRN 2146844;2,2-Dichloro-N-(3-chloro-1,4-dihydro-1,4-dioxo-2-naphthalenyl)acetamide;2,2-Dichloro-N-(3-chloronaphthoquinon-2-yl)acetamide;UNII-618QV11Q2U;2,2-Dichloro-N-(3-chloro-1,4-naphthoquinon-2-yl)acetamide;618QV11Q2U;Acetamide, 2,2-dichloro-N-(3-chloro-1,4-dihydro-1,4-dioxo-2-naphthalenyl)-;Acetamide, 2,2-dichloro-N-(3-chloro-1,4-dihydro-1,4-dioxo-2-naphthyl)-;SCHEMBL134428;DTXSID2058047;CHEBI:82175;LS-8847;Quinonamid, PESTANAL(R), analytical standard;C19048;J-016809;Q27155784;ACETAMIDE, 2,2-DICHLORO-N-(3-CHLORO-1,4-DIHYDRO-1,4-DIOXO-2- NAPHTHYL)-;Acetamide, 2,2-dichloro-N-(3-chloro-1,4-dihydro-1,4-dioxo-2-naphthalenyl)- [

Chemical Property of Quinonamid

Chemical Property:

• Vapor Pressure: 1.34E-08mmHg at 25°C
• Melting Point: 212.5°C
• Boiling Point: 458.8°Cat760mmHg
• PKA: 7.37±0.20(Predicted)
• Flash Point: 231.3°C
• PSA: 63.24000
• Density: 1.62g/cm³
• LogP: 2.82680
• Water Solubility.: 3mg/L(23 oC)
• XLogP3: 3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 316.941326
• Heavy Atom Count: 19
• Complexity: 473

Purity/Quality:

98%Min ^*data from raw suppliers

Safty Information:

• Safety Statements: 22-24/25

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C2C(=C1)C(=O)C(=C(C2=O)Cl)NC(=O)C(Cl)Cl
• Uses: Quinonamid is an antiparasitic agent, an algicide.

Technology Process of Quinonamid

There total 1 articles about Quinonamid 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:

→ 2-Chloro-3-dichloroacetylamino-1,4-naphthoquinone (27541-88-4)

Guidance literature:

entspr. Amin, (Cl2CH-CO)2O;

Reference yield: 76.0%

2-Chloro-3-dichloroacetylamino-1,4-naphthoquinone (27541-88-4) + aniline (62-53-3) → 2-Anilino-3-dichloracetylamino-1,4-naphthochinon (136197-69-8)

Guidance literature:

In ethanol; Heating;

Reference yield: 71.0%

2-Chloro-3-dichloroacetylamino-1,4-naphthoquinone (27541-88-4) + o-toluidine (95-53-4) → 2-Dichloroacetylamino-3-(2-methylanilino)-1,4-naphthoquinone (137681-73-3)

Guidance literature:

In ethanol; Heating;

Downstream raw materials:

2-Dichloracetyl-3-(4-hydroxyanilino)-1,4-naphthochinon

2-Dichloracetylamino-3-(4-chloranilino)-1,4-naphthochinon

2-Anilino-3-dichloracetylamino-1,4-naphthochinon

2-Dichloroacetylamino-3-(2-methylanilino)-1,4-naphthoquinone