Transfluthrin

Base Information

• Chemical Name: Transfluthrin
• CAS No.: 118712-89-3
• Molecular Formula: C15H12Cl2F4O2
• Molecular Weight: 371.159
• Hs Code.: 29162090
• European Community (EC) Number: 405-060-5,635-009-4
• UNII: QWL3SKA6EG
• DSSTox Substance ID: DTXSID4046812
• Nikkaji Number: J866.718G
• Wikipedia: Transfluthrin
• Wikidata: Q418421
• Metabolomics Workbench ID: 54522
• ChEMBL ID: CHEMBL3184657
• Mol file: 118712-89-3.mol

Synonyms:2,3,5,6-tetrafluorobenzyl (+)-(1R-trans)-2,2-dimethyl-3-(2,2-dichlorovinyl)cyclopropanecarboxylate;transfluthrin

Chemical Property of Transfluthrin

Chemical Property:

• Appearance/Colour: colorless crystals
• Vapor Pressure: 4.12E-05mmHg at 25°C
• Melting Point: 32oC
• Refractive Index: 1.549
• Boiling Point: 351.4 °C at 760 mmHg
• Flash Point: 115.5 °C
• PSA: 26.30000
• Density: 1.492 g/cm³
• LogP: 4.87740
• XLogP3: 5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 5
• Exact Mass: 370.0150477
• Heavy Atom Count: 23
• Complexity: 482

Purity/Quality:

93% ^*data from raw suppliers

Transfluthrin ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi,N
• Hazard Codes: Xi;N,N,Xi
• Statements: 38-50/53
• Safety Statements: 36/37-60-61

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1(C(C1C(=O)OCC2=C(C(=CC(=C2F)F)F)F)C=C(Cl)Cl)C
• Isomeric SMILES: CC1([C@@H]([C@H]1C(=O)OCC2=C(C(=CC(=C2F)F)F)F)C=C(Cl)Cl)C
• Uses: Transfluthrin is a fluorinated aromatic compound for proteomics research.

Technology Process of Transfluthrin

There total 2 articles about Transfluthrin 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: 97.6%

(1R)-trans-3-(2,2-dichloro-1-ethenyl)-2,2-dimethylcyclopropanecarboxylic acid chloride (61914-47-4) + (2,3,5,6-tetrafluorophenyl)methanol (4084-38-2) → transfluthrin (118712-89-3)

Guidance literature:

With pyridine; In toluene; at 5 - 15 ℃; for 3h;

Reference yield:

→ transfluthrin (118712-89-3)

Guidance literature:

upstream raw materials:

(1R)-trans-3-(2,2-dichloro-1-ethenyl)-2,2-dimethylcyclopropanecarboxylic acid chloride

(2,3,5,6-tetrafluorophenyl)methanol

Refernces

• 1、 -. "2,3,5,6-Tetrafluorobenzyl (+) 1r-trans-2,2-dimethyl-3-(2,2-dichlorovinyl)-cyclopropanecarboxylate". . . Retrieved 2008/06/13.