Chlorflurecol

Base Information

• Chemical Name: Chlorflurecol
• CAS No.: 2464-37-1
• Molecular Formula: C14H9ClO3
• Molecular Weight: 260.677
• Hs Code.: 29181990
• European Community (EC) Number: 219-565-1
• NSC Number: 102385
• UNII: G63PIX99OZ
• DSSTox Substance ID: DTXSID2034251
• Nikkaji Number: J7.582E
• Wikidata: Q27278817
• ChEMBL ID: CHEMBL1904254
• Mol file: 2464-37-1.mol

Synonyms:chlorflurenol

Chemical Property of Chlorflurecol

Chemical Property:

• Vapor Pressure: 8.14E-12mmHg at 25°C
• Melting Point: 152 °C
• Refractive Index: 1.719
• Boiling Point: 524.184 °C at 760 mmHg
• PKA: 3.09±0.20(Predicted)
• Flash Point: 270.817 °C
• PSA: 57.53000
• Density: 1.552 g/cm³
• LogP: 2.64090
• Storage Temp.: 2-8°C
• XLogP3: 2.6
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 260.0240218
• Heavy Atom Count: 18
• Complexity: 359

Purity/Quality:

99% ^*data from raw suppliers

Chlorflurenol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Pesticides -> Herbicides, Other
• Canonical SMILES: C1=CC=C2C(=C1)C3=C(C2(C(=O)O)O)C=C(C=C3)Cl
• Uses: Chlorflurenol is a pesticide.

Technology Process of Chlorflurecol

There total 2 articles about Chlorflurecol 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-9,10-phenanthrenequinone (56961-98-9) → chloroflurenol (2464-37-1)

Guidance literature:

With potassium hydroxide;

DOI:10.1002/jsfa.2740050106

Reference yield:

→ chloroflurenol (2464-37-1)

Guidance literature:

upstream raw materials:

2-chloro-9,10-phenanthrenequinone

Refernces

• 1、 -. "1,2,3-Thiadiazole-3-in-5-ylidene-urea derivatives, process for making the same and compositions containing the same having growth regulating activity for plants". . . Retrieved 2008/06/13.